Disease Name Symbol Acronym
Macdermot-Winter Syndrome MCD004
Machado-Joseph Disease MCH002 SCA3
Machado-Joseph Disease Type 1 MCH012
Machado-Joseph Disease Type 2 MCH014
Machado-Joseph Disease Type 3 MCH013
Macrocephaly and Epileptic Encephalopathy MCR347
Macrocephaly Mesodermal Hamartoma Spectrum MCR030
Macrocephaly, Benign Familial MCR031
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation MCR321 MDFPMR
Macrocephaly, Macrosomia, and Facial Dysmorphism Syndrome MCR353 MMFD
Macrocephaly/autism Syndrome MCR096 MCEPHAS
Macrocephaly/megalencephaly Syndrome, Autosomal Recessive MCR237 MGCPH
Macrocephaly-Short Stature-Paraplegia Syndrome MCR294
Macrocystic Neurilemmoma MCR002
Macrocystic Pattern Testicular Yolk Sac Tumor MCR003
Macrocytic Anemia MCR017
Macrocytosis, Familial MCR339
Macrodactyly MCR364
Macrodactyly of Fingers MCR184
Macrodactyly of Fingers, Bilateral MCR187
Macrodactyly of Fingers, Unilateral MCR188
Macrodactyly of the Foot MCR034
Macrodactyly of the Hand MCR035
Macrodactyly of Toes MCR185
Macrodactyly of Toes, Bilateral MCR189
Macrodactyly of Toes, Unilateral MCR190
Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance MCR036
Macroglobulinemia MCR004
Macroglobulinemia, Waldenstrom 1 MCR161 WM1
Macroglobulinemia, Waldenstrom 2 MCR162 WM2
Macroglossia MCR037
Macrophage Activation Syndrome MCR225
Macrophagic Myofasciitis MCR039 MMF
Macrophthalmia, Colobomatous, with Microcornea MCR317 MACOM
Macrosomia Adiposa Congenita MCR332
Macrosomia with Microphthalmia, Lethal MCR303
Macrostomia, Isolated MCR302
Macrostomia-Preauricular Tags-External Ophthalmoplegia Syndrome MCR301
Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss MCR359 MATINS
Macrothrombocytopenia Progressive Deafness MCR041
Macrothrombocytopenia with Mitral Valve Insufficiency MCR178
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related MCR125 MAD-TUBB1
Macrotrabecular Hepatoblastoma MCR005
Macrozoospermia MCR265 SPGF5
Macs Syndrome MCS006 MACS
Macular Amyloidosis MCL047
Macular Degeneration, Age-Related, 1 MCL042 ARMD1
Macular Degeneration, Age-Related, 10 MCL030 ARMD10
Macular Degeneration, Age-Related, 11 MCL032 ARMD11
Macular Degeneration, Age-Related, 12 MCL051 ARMD12
Macular Degeneration, Age-Related, 13 MCL052 ARMD13
Macular Degeneration, Age-Related, 14 MCL078 ARMD14
Macular Degeneration, Age-Related, 15 MCL065 ARMD15
Macular Degeneration, Age-Related, 2 MCL043 ARMD2
Macular Degeneration, Age-Related, 4 MCL038 ARMD4
Macular Degeneration, Age-Related, 5 MCL077 ARMD5
Macular Degeneration, Age-Related, 6 MCL036 ARMD6
Macular Degeneration, Age-Related, 7 MCL041 ARMD7
Macular Degeneration, Age-Related, 8 MCL039 ARMD8
Macular Degeneration, Age-Related, 9 MCL044 ARMD9
Macular Degeneration, Early-Onset MCL058 EOMD
Macular Degeneration, X-Linked Atrophic MCL029 MDXLA
Macular Dystrophy with Central Cone Involvement MCL057 CCMD
Macular Dystrophy, Concentric Annular MCL018 BCAMD
Macular Dystrophy, Corneal MCL075 MCD
Macular Dystrophy, Dominant Cystoid MCL027 CYMD
Macular Dystrophy, Fenestrated Sheen Type MCL074
Macular Dystrophy, Patterned, 1 MCL059 MDPT1
Macular Dystrophy, Patterned, 2 MCL071 MDPT2
Macular Dystrophy, Patterned, 3 MCL070 MDPT3
Macular Dystrophy, Retinal, 1, North Carolina Type MCL069 NCMD
Macular Dystrophy, Retinal, 2 MCL035 MCDR2
Macular Dystrophy, Retinal, 3 MCL026 MCDR3
Macular Dystrophy, Vitelliform, 1 MCL073 VMD1
Macular Dystrophy, Vitelliform, 2 MCL066 VMD2
Macular Dystrophy, Vitelliform, 3 MCL060 VMD3
Macular Dystrophy, Vitelliform, 4 MCL061 VMD4
Macular Dystrophy, Vitelliform, 5 MCL056 VMD5
Macular Dystrophy, X-Linked MCL076
Macular Holes MCL003
Macular Keratitis MCL004
Macular Retinal Edema MCL006
Macular Telangiectasia Type 2 MCL079 IJT
Macules Hereditary Congenital Hypopigmented and Hyperpigmented MCL020
Madelung Deformity MDL024
Madelung Deformity, Bilateral MDL017
Madelung Deformity, Unilateral MDL018
Madokoro Ohdo Sonoda Syndrome MDK001
Madras Motor Neuron Disease MDR004 MMND
Magic Syndrome MGC006
Magnesium, Elevated Red Cell MGN003
Mahvash Disease MHV001
Main Bronchus Cancer MNB001
Majeed Syndrome MJD001 MJDS
Major Affective Disorder 1 MJR007 MD1
Major Affective Disorder 2 MJR008 MDI
Major Affective Disorder 3 MJR021 BPEO
Major Affective Disorder 4 MJR004 BPAD
Major Affective Disorder 5 MJR006 BPAD
Major Affective Disorder 6 MJR003 BPAD
Major Affective Disorder 7 MJR023 MAFD7
Major Affective Disorder 8 MJR022 MAFD8
Major Affective Disorder 9 MJR024 MAFD9
Major Depressive Disorder MJR001 MDD
Major Depressive Disorder 1 MJR013 MDD1
Major Depressive Disorder 2 MJR014 MDD2
Mal De Debarquement Syndrome MLD017 MDD
Mal De Meleda MLD006 MDM
Malakoplakia MLK004
Malaria MLR004 CM
Malaria, Mild MLR020 MAL
Male Genital Organ Stricture MLG025
Male Genital Organ Vascular Disease MLG026
Male Infertility MLN007
Male Infertility with Spermatogenesis Disorder MLN061
Male Infertility with Spermatogenesis Disorder Due to Single Gene Mutation MLN062
Male Infertility with Teratozoospermia Due to Single Gene Mutation MLN056
Male Pseudohermaphroditism Due to Defective Lh Molecule MLP002
Male Pseudohermaphroditism Intellectual Disability Syndrome, Verloes Type MLP003
Male Pseudohermaphroditism/mental Retardation Syndrome, Verloes Type MLP006
Male Reproductive Organ Benign Neoplasm MLR005
Male Reproductive Organ Cancer MLR006
Male Reproductive System Disease MLR007
Male Urethral Cancer MLR008
Maleic Anhydride Allergic Asthma MLC007
Maleylacetoacetate Isomerase Deficiency MLY011 MAAID
Maligant Granulosa Cell Tumor of the Ovary MLG155
Malignancy Diagnosed During Pregnancy MLG118
Malignant Acrospiroma MLG048
Malignant Acth Producing Neoplasm of Pituitary Gland MLG046
Malignant Adenofibroma MLG060
Malignant Adult Ependymoma MLG023
Malignant Anus Melanoma MLG038
Malignant Atrophic Papulosis MLG141
Malignant Biphasic Mesothelioma MLG011
Malignant Breast Melanoma MLG008
Malignant Cardiac Germ Cell Tumor MLG058
Malignant Cardiac Peripheral Nerve Sheath Neoplasm MLG057
Malignant Childhood Germ Cell Neoplasm MLG037
Malignant Choroid Melanoma MLG061
Malignant Ciliary Body Melanoma MLG062
Malignant Conjunctival Melanoma MLG142
Malignant Cornea Melanoma MLG052
Malignant Cylindroma MLG087
Malignant Cystadenoma MLG158
Malignant Cystic Nephroma MLG055
Malignant Dermis Tumor MLG063
Malignant Dysgerminomatous Germ Cell Tumor of the Ovary MLG156
Malignant Ectomesenchymoma MLG133
Malignant Ependymoma MLG064
Malignant Epithelial Mesothelioma MLG012
Malignant Epithelial Tumor of Salivary Glands MLG134
Malignant Epithelioid Hemangioendothelioma MLG145
Malignant Essential Hypertension MLG039
Malignant Eyelid Melanoma MLG010
Malignant Fibrous Histiocytoma of Bone MLG014
Malignant Fibroxanthoma MLG065 MFH
Malignant Gastric Germ Cell Tumor MLG066
Malignant Gastric Granular Cell Tumor MLG044
Malignant Gastric Teratoma MLG024
Malignant Germ Cell Tumor of the Cervix Uteri MLG117
Malignant Germ Cell Tumor of the Corpus Uteri MLG114
Malignant Germ Cell Tumor of the Vagina MLG146
Malignant Giant Cell Tumor MLG067
Malignant Giant Cell Tumor of Soft Parts MLG018
Malignant Giant Cell Tumor of the Tendon Sheath MLG019
Malignant Glandular Tumor of Peripheral Nerve Sheath MLG051
Malignant Glioma MLG068
Malignant Granular Cell Esophageal Tumor MLG031
Malignant Granular Cell Myoblastoma MLG032
Malignant Granular Cell Skin Tumor MLG050
Malignant Growth Hormone Secreting Neoplasm of Pituitary MLG045
Malignant Hemangioma MLG144
Malignant Histiocytic Disease MLG020
Malignant Histiocytosis MLG054
Malignant Hypertension MLG069
Malignant Hypertensive Renal Disease MLG004
Malignant Hyperthermia MLG056 MH
Malignant Hyperthermia 1 MLG147 MHS1
Malignant Hyperthermia 2 MLG148 MHS2
Malignant Hyperthermia 3 MLG149 MHS3
Malignant Hyperthermia 4 MLG150 MHS4
Malignant Hyperthermia 5 MLG151 MHS5
Malignant Hyperthermia 6 MLG152 MHS6
Malignant Hyperthermia Arthrogryposis Torticollis MLG089
Malignant Hyperthermia of Anesthesia MLG143
Malignant Hyperthermia Susceptibility MLG086
Malignant Iris Melanoma MLG070
Malignant Leptomeningeal Tumor MLG071
Malignant Leydig Cell Tumor MLG072
Malignant Mediastinal Neurogenic Neoplasm MLG125
Malignant Mediastinum Hemangiopericytoma MLG043
Malignant Melanocytic Neoplasm of the Peripheral Nerve Sheath MLG073
Malignant Melanocytic Peripheral Nerve Sheath Tumor of Mediastinum MLG015
Malignant Melanoma of the Mucosa MLG109
Malignant Melanoma, Childhood MLG096
Malignant Mesenchymoma MLG074
Malignant Migrating Partial Seizures of Infancy MLG120 MPEI
Malignant Neoplasm of Acoustic Nerve MLG028
Malignant Neoplasm of Short Bones of Lower Limb MLG006
Malignant Non-Dysgerminomatous Germ Cell Tumor of Ovary MLG127
Malignant Oculomotor Nerve Tumor MLG027
Malignant Otitis Externa MLG042
Malignant Ovarian Brenner Tumor MLG053
Malignant Ovarian Cyst MLG033
Malignant Ovarian Mixed Epithelial Neoplasm MLG035
Malignant Ovarian Surface Epithelial-Stromal Neoplasm MLG076
Malignant Parietal Pleura Tumor MLG030
Malignant Peripheral Nerve Sheath Tumor MLG077 MPNST
Malignant Peripheral Nerve Sheath Tumor with Perineurial Differentiation MLG153
Malignant Peritoneal Mesothelioma MLG002
Malignant Peritoneal Solitary Fibrous Tumor MLG013
Malignant Pheochromocytoma MLG157
Malignant Pineal Area Germ Cell Neoplasm MLG078
Malignant Pleural Mesothelioma MLG079
Malignant Pleural Solitary Fibrous Tumor MLG001
Malignant Renovascular Hypertension MLG003
Malignant Secondary Hypertension MLG080
Malignant Sertoli Cell Tumor MLG022
Malignant Sertoli-Leydig Cell Tumor MLG021
Malignant Sertoli-Leydig Cell Tumor of the Ovary MLG154
Malignant Skin Fibrous Histiocytoma MLG007
Malignant Spindle Cell Melanoma MLG005
Malignant Spiradenoma MLG036 MES
Malignant Struma Ovarii MLG059
Malignant Syringoma MLG049
Malignant Teratocarcinosarcoma MLG099
Malignant Teratoma MLG081
Malignant Testicular Leydig Cell Tumor MLG009
Malignant Thyroid Stimulating Hormone Producing Neoplasm of Pituitary Gland MLG047
Malignant Triton Tumor MLG041 MTT
Malignant Tumor of Undescended Testis MLG017
Malignant Type a Thymoma MLG034
Malignant Type Ab Thymoma MLG040
Malignant Visceral Pleura Tumor MLG029
Mallory-Weiss Syndrome MLL004
Malocclusion and Short Stature MLC006
Malocclusion Due to Protuberant Upper Front Teeth MLC005
Malonyl-Coa Decarboxylase Deficiency MLN011 MLYCD DEFICIENCY
Malposition of Teeth with or Without Hypodontia/oligodontia MLP007
Malposition of the Coronary Ostium MLP005
Malt Worker's Lung MLT013
Mammary Paget's Disease MMM001
Mammary-Digital-Nail Syndrome MMM002 MDNS
Mammastatin MMM005
Mammographic Density MMM006
Man1b1-Cdg MN1002
Mandibular Arteriovenous Malformation MND008
Mandibular Cancer MND001
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome MND021 MDPL
Mandibuloacral Dysplasia with Type a Lipodystrophy MND003 MADA
Mandibuloacral Dysplasia with Type B Lipodystrophy MND002 MADB
Mandibulofacial Dysostosis Syndrome, Bauru Type MND029
Mandibulofacial Dysostosis with Alopecia MND025 MFDA
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia MND027 MEHM
Mandibulofacial Dysostosis with Mental Retardation MND028
Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant MND030
Mandibulofacial Dysostosis, Guion-Almeida Type MND020 MFDM
Manganese Poisoning MNG007
Manitoba Oculotrichoanal Syndrome MNT006 MOTA
Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type MNN046
Mannose-Binding Lectin Deficiency MNN034 MBLD
Mannose-Binding Lectin Protein Deficiency MNN041
Mannosidosis MNN018
Mannosidosis, Alpha B, Lysosomal MNN047 MANSA
Mannosidosis, Beta a, Lysosomal MNN019 MANSB
Manouvrier Syndrome MNV001
Mansonelliasis MNS001
Mantle Cell Lymphoma MNT001 LCM
Maple Bark Strippers' Lung MPL002
Maple Syrup Urine Disease MPL001 MSUD
Maple Syrup Urine Disease, Mild Variant MPL011 MSUDMV
Mapt-Related Disorders MPT001
Marantic Endocarditis MRN001
Marasmus MRS001
Marburg Acute Multiple Sclerosis MRB005
Marburg Hemorrhagic Fever MRB001 MHF
Marchiafava Bignami Disease MRC001 MBD
Marcus Gunn Phenomenon MRC002
Marden Walker Like Syndrome MRD001 VDEGS
Marden-Walker Syndrome MRD002 MWKS
Marek Disease MRK002
Marfan Lipodystrophy Syndrome MRF019 MFLS
Marfan Syndrome MRF001 MFS
Marfanoid Habitus with Microcephaly and Glomerulonephritis MRF018
Marfanoid Habitus with Situs Inversus MRF020
Marfanoid Habitus-Autosomal Recessive Intellectual Disability Syndrome MRF015
Marfanoid Habitus-Inguinal Hernia-Advanced Bone Age Syndrome MRF016
Marfanoid Hypermobility Syndrome MRF007
Marfanoid Mental Retardation Syndrome, Autosomal MRF017
Marginal Corneal Ulcer MRG002
Marginal Glioneuronal Heterotopia MRG004
Marginal Zone B-Cell Lymphoma MRG003 MZL
Marie Unna Congenital Hypotrichosis MRN005 MUHH
Marin-Amat Syndrome MRN008
Marinesco-Sjogren Syndrome MRN003 MSS
Marinesco-Sjogren-Like Syndrome MRN006
Markel Vikkula Mulliken Syndrome MRK003
Maroteaux Fonfria Syndrome MRT004
Maroteaux Stanescu Cousin Syndrome MRT005
Marphanoid Syndrome Type De Silva MRP003
Marsden Nyhan Sakati Syndrome MRS003
Marshall Syndrome MRS002 MRSHS
Marshall-Smith Syndrome MRS004 MRSHSS
Marsili Syndrome MRS009 MARSIS
Martinez Monasterio Pinheiro Syndrome MRT006
Martinez-Frias Syndrome MRT009
Martsolf Syndrome MRT007 MARTS
Masa Syndrome MSS001 SPG1
Masp2 Deficiency MSP001 MASPD
Mass Syndrome MSS002 OCTD
Massa Casaer Ceulemans Syndrome MSS003
Mast Cell Activation Syndrome MST020 MCAS
Mast Cell Neoplasm MST004
Mast Syndrome MST006 SPG21
Mast-Cell Leukemia MST002
Mast-Cell Sarcoma MST001
Masters-Allen Syndrome MST003
Masticatory Muscles, Hypertrophy of MST022
Mastitis MST005
Mastocytic Enterocolitis MST008
Mastocytosis MST009
Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia MST010
Mastocytosis, Cutaneous MST024 MASTC
Mastoiditis MST019
Mastroiacovo De Rosa Satta Syndrome MST011
Mastroiacovo Gambi Segni Syndrome MST012
Maternal Hyperphenylalaninemia MTR016 MPKU
Maternal Hyperthermia Induced Birth Defects MTR050
Maternal Uniparental Disomy of Chromosome 1 MTR051
Maternal Uniparental Disomy of Chromosome 13 MTR079
Maternal Uniparental Disomy of Chromosome 16 MTR067
Maternal Uniparental Disomy of Chromosome 2 MTR063
Maternal Uniparental Disomy of Chromosome 21 MTR065
Maternal Uniparental Disomy of Chromosome 22 MTR064
Maternal Uniparental Disomy of Chromosome 4 MTR062
Maternal Uniparental Disomy of Chromosome 6 MTR061
Maternal Uniparental Disomy of Chromosome 9 MTR060
Maternal Uniparental Disomy of Chromosome X MTR057
Maternally-Inherited Cardiomyopathy and Hearing Loss MTR049
Maternally-Inherited Mitochondrial Dystonia MTR052
Maternally-Inherited Progressive External Ophthalmoplegia MTR058
Matsoukas Liarikos Giannika Syndrome MTS003
Mature B-Cell Neoplasm MTR008
Mature Cataract MTR001
Mature Gastric Teratoma MTR006
Mature Teratoma MTR010
Mature Teratoma of the Ovary MTR011
Maturity-Onset Diabetes of the Young MTR004 MODY
Maturity-Onset Diabetes of the Young, Type 1 MTR018 MODY1
Maturity-Onset Diabetes of the Young, Type 10 MTR044 MODY10
Maturity-Onset Diabetes of the Young, Type 11 MTR039 MODY11
Maturity-Onset Diabetes of the Young, Type 13 MTR075 MODY13
Maturity-Onset Diabetes of the Young, Type 14 MTR074 MODY14
Maturity-Onset Diabetes of the Young, Type 2 MTR019 MODY2
Maturity-Onset Diabetes of the Young, Type 3 MTR020 MODY3
Maturity-Onset Diabetes of the Young, Type 4 MTR021 MODY4
Maturity-Onset Diabetes of the Young, Type 6 MTR023 MODY6
Maturity-Onset Diabetes of the Young, Type 7 MTR024 MODY7
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction MTR082 MODY8
Maturity-Onset Diabetes of the Young, Type 9 MTR026 MODY9
Maumenee Syndrome MMN001
Maxillary Arteriovenous Malformation MXL013
Maxillary Cancer MXL017
Maxillary Double Lip MXL010
Maxillary Sinus Adenocarcinoma MXL006
Maxillary Sinus Adenoid Cystic Carcinoma MXL002
Maxillary Sinus Cancer MXL008
Maxillary Sinus Cholesteatoma MXL007
Maxillary Sinus Inverted Papilloma MXL005
Maxillary Sinus Schneiderian Papilloma MXL003
Maxillary Sinus Squamous Cell Carcinoma MXL004
Maxillary Sinusitis MXL015
Maxillofacial Dysostosis MXL011
Maxillonasal Dysplasia, Binder Type MXL016
Mayer-Rokitansky-Kuster-Hauser Syndrome MYR002 RKH SYNDROME
May-Thurner Syndrome MYT019
Mazabraud Syndrome MZB001
Mbd25-Related Intellectual Disability MBD002
Mbd5 Haploinsufficiency MBD001 MAND
Mccallum Macadam Johnston Syndrome MCC006
Mccune-Albright Syndrome MCC012 MAS
Mcdonough Syndrome MCD002
Mcdowall Syndrome MCD003
Mcgillivray Syndrome MCG001
Mckusick-Kaufman Syndrome MCK005 MKKS
Mcleod Syndrome MCL009 MLS
Mcpherson Clemens Syndrome MCP018
Mcpherson Robertson Cammarano Syndrome MCP019
Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency MCT002
Mda5 Deficiency MD5001
Mdp Syndrome MDP002
Meacham Syndrome MCH011 MEACHS
Meacham Winn Culler Syndrome MCH007
Mean Platelet Volume Quantitative Trait Locus 1 MNP014
Mean Platelet Volume Quantitative Trait Locus 2 MNP015
Mean Platelet Volume Quantitative Trait Locus 3 MNP016
Mean Platelet Volume Quantitative Trait Locus 4 MNP019
Mean Platelet Volume Quantitative Trait Locus 5 MNP020
Mean Platelet Volume Quantitative Trait Locus 6 MNP021
Measles MSL001
Mechanical Ectropion MCH001
Mechanical Entropion MCH004
Mechanical Lagophthalmos MCH005
Mechanical Strabismus MCH006
Meckel Diverticulum MCK029
Meckel Syndrome 12 MCK026 MKS12
Meckel Syndrome 13 MCK028 MKS13
Meckel Syndrome, Type 1 MCK013 MKS1
Meckel Syndrome, Type 10 MCK035 MKS10
Meckel Syndrome, Type 11 MCK020 MKS11
Meckel Syndrome, Type 2 MCK031 MKS2
Meckel Syndrome, Type 3 MCK032 MKS3
Meckel Syndrome, Type 4 MCK033 MKS4
Meckel Syndrome, Type 5 MCK014 MKS5
Meckel Syndrome, Type 6 MCK012 MKS6
Meckel Syndrome, Type 7 MCK030 MKS7
Meckel Syndrome, Type 8 MCK034 MKS8
Meckel Syndrome, Type 9 MCK036 MKS9
Meckel's Diverticulitis MCK004
Meckel's Diverticulum Cancer MCK001
Meconium Aspiration Syndrome MCN007 MAS
Meconium Ileus MCN017 MECIL
Mecp2-Related Disorders MCP017
Mecp2-Related Severe Neonatal Encephalopathy MCP022
Med12-Related Disorders MD1001
Med13l Haploinsufficiency Syndrome MD1003
Med23 MD2001 MED23
Medeira-Dennis-Donnai Syndrome MDR001
Medial Medullary Syndrome MDL007 MMS
Median Arcuate Ligament Syndrome MDN008 MALS
Median Cleft Lip/mandibule MDN007
Median Cleft of the Upper Lip and Maxilla MDN006
Median Neuropathy MDN002
Median Rhomboid Glossitis MDN001
Median-Ulnar Nerve Communications MDN009
Mediastinal Cancer MDS018
Mediastinal Endodermal Sinus Tumors MDS024 EST
Mediastinal Granular Cell Myoblastoma MDS005
Mediastinal Gray Zone Lymphoma MDS006
Mediastinal Lipomatosis MDS003
Mediastinal Malignant Lymphoma MDS019
Mediastinal Melanocytic Neurilemmoma MDS016
Mediastinal Mesenchymal Tumor MDS012
Mediastinal Neurilemmoma MDS020
Mediastinal Osteogenic Sarcoma MDS009
Mediastinitis MDS022
Mediastinum Angiosarcoma MDS001
Mediastinum Ganglioneuroblastoma MDS013
Mediastinum Leiomyoma MDS004
Mediastinum Leiomyosarcoma MDS017
Mediastinum Liposarcoma MDS002
Mediastinum Neuroblastoma MDS014
Mediastinum Neurofibroma MDS007
Mediastinum Rhabdomyosarcoma MDS008
Mediastinum Sarcoma MDS023
Mediastinum Seminoma MDS010
Mediastinum Synovial Sarcoma MDS015
Mediastinum Teratoma MDS011
Medich Giant Platelet Syndrome MDC003
Mediosternal Depigmentation Line MDS027
Medium Chain 3-Ketoacyl-Coa Thiolase Deficiency MDM005
Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency MDM001 MCADD
Medrano Roldan Syndrome MDR002
Medullary Colon Carcinoma MDL026
Medullary Cystic Kidney Disease 1 MDL008 MCKD1
Medullary Cystic Kidney Disease 2 MDL021 MCKD2
Medullary Sponge Kidney MDL009 MSK
Medulloadrenal Hyperfunction MDL001
Medulloblastoma MDL005 MDB
Medulloepithelioma MDL002
Medullomyoblastoma MDL003
Meester-Loeys Syndrome MST021 MRLS
Megacolon MGC001
Megacystis-Megaureter Syndrome MGC005
Megaepiphyseal Dwarfism MGP001
Megaesophagus MGS001
Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) MGK005
Megakaryocytic Leukemia MGK001 AMKL
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 MGL009 MLC1
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a MGL010 MLC2A
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b, Remitting, with or Without Mental Retardation MGL011 MLC2B
Megalencephaly MGL013
Megalencephaly with Dysmyelination MGL037
Megalencephaly, Autosomal Dominant MGL035
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome MGL038 MCAP
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 MGL030 MPPH1
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 MGL028 MPPH2
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 MGL029 MPPH3
Megaloblastic Anemia MGL001 IGS
Megaloblastic Anemia 1 MGL018 RH-MGA1
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency MGL012 DHFRD
Megalocornea MGL003
Megalocornea - Spherophakia - Secondary Glaucoma MGL005 MSPKA
Megalocornea-Intellectual Disability Syndrome MGL027
Megalocornea-Mental Retardation Syndrome MGL033
Megalocytic Interstitial Nephritis MGL007
Megarbane Syndrome MGR005
Megarbane-Jalkh Syndrome MGR041
Mehes Syndrome MHS001
Mehmo Syndrome MHM001 MEHMO
Mehta Lewis Patton Syndrome MHT001
Meibomian Cyst MBM001
Meier-Gorlin Syndrome 1 MRG008 MGORS1
Meier-Gorlin Syndrome 2 MRG009 MGORS2
Meier-Gorlin Syndrome 3 MRG010 MGORS3
Meier-Gorlin Syndrome 4 MRG011 MGORS4
Meier-Gorlin Syndrome 5 MRG012 MGORS5
Meier-Gorlin Syndrome 6 MRG014 MGORS6
Meier-Gorlin Syndrome 7 MRG015 MGORS7
Meier-Gorlin Syndrome 8 MRG016 MGORS8
Meinecke Syndrome MNC010
Melancholia MLN003
Melanoacanthoma MLN005
Melanocytic Lesions of Cns MLN015
Melanocytic Nevus Syndrome, Congenital MLN065 CMNS
Melanocytic Psammomatous Mpnst MLN006
Melanoma MLN008
Melanoma Metastasis MLN013
Melanoma of Soft Tissue MLN064
Melanoma Tumor Antigen Gp90 MLN071 GP90
Melanoma, Cutaneous Malignant 1 MLN066 CMM
Melanoma, Cutaneous Malignant 10 MLN055 CMM10
Melanoma, Cutaneous Malignant 2 MLN067 CMM2
Melanoma, Cutaneous Malignant 3 MLN075 CMM3
Melanoma, Cutaneous Malignant 4 MLN074 CMM4
Melanoma, Cutaneous Malignant 5 MLN076 CMM5
Melanoma, Cutaneous Malignant 6 MLN042 CMM6
Melanoma, Cutaneous Malignant 7 MLN040 CMM7
Melanoma, Cutaneous Malignant 8 MLN043 CMM8
Melanoma, Cutaneous Malignant 9 MLN077 CMM9
Melanoma, Malignant Familial Intraocular MLN068
Melanoma, Uveal MLN069
Melanoma, Uveal 1 MLN039 UVM1
Melanoma, Uveal 2 MLN041 UVM2
Melanoma-Associated Retinopathy MLN046
Melanoma-Astrocytoma Syndrome MLN070 MASTS
Melanoma-Pancreatic Cancer Syndrome MLN047 FAMMMPC
Melanomatosis MLN002
Melanosis, Neurocutaneous MLN073 NCMS
Melanotic Medulloblastoma MLN004
Melanotic Neurilemmoma MLN009
Melanotic Neuroectodermal Tumor MLN001
Melhem Fahl Syndrome MLH001
Melioidosis MLD001
Melkersson-Rosenthal Syndrome MLK003 MRS
Melnick-Needles Syndrome MLN014 MNS
Melon Allergy MLN063
Melorheostosis MLR003
Melorheostosis with Osteopoikilosis MLR010
Melorheostosis, Isolated MLR023 MEL
Melphalan Allergy MLP008
Membranoproliferative Glomerulonephritis MMB001 MPGN
Membranoproliferative Glomerulonephritis, X-Linked MMB013
Membranous Cranial Ossification, Delayed MMB012
Membranous Nephropathy MMB011 MGN
Memory Quantitative Trait Locus MMR005
Menarche, Age at, Quantitative Trait Locus 1 MNR013
Menarche, Age at, Quantitative Trait Locus 2 MNR014
Menarche, Age at, Quantitative Trait Locus 3 MNR015
Mend Syndrome MND023 MEND
Meniere Disease MNR012
Meningeal Melanocytoma MNN001
Meningeal Melanoma MNN010
Meningeal Melanomatosis MNN008
Meninges Hemangiopericytoma MNN006
Meninges Sarcoma MNN011
Meningioma, Familial MNN043 MNGMA
Meningioma, Radiation-Induced MNN042 MNRI
Meningitis MNN013
Meningitis and Encephalitis MNN024
Meningocele MNN007
Meningococcal Infection MNN020
Meningococcal Meningitis MNN032
Meningococcemia MNN021
Meningoencephalitis MNN009
Meningoencephalocele MNN022
Meningothelial Meningioma MNN004
Meningovascular Neurosyphilis MNN005
Menkes Disease MNK001 MNKD
Menopause, Natural, Age at, Quantitative Trait Locus 1 MNP013
Menopause, Natural, Age at, Quantitative Trait Locus 2 MNP017
Menopause, Natural, Age at, Quantitative Trait Locus 4 MNP018
Mental and Growth Retardation with Amblyopia MNT299
Mental Depression MNT002
Mental Health Wellness 1 MNT312 MHW1
Mental Health Wellness 2 MNT313 MHW2
Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects MNT266 MRFACD
Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia MNT046 MICPCH
Mental Retardation and Psoriasis MNT255
Mental Retardation Macrocephaly Coarse Facies Hypotonia MNT020
Mental Retardation Short Stature Microcephaly Eye MNT026
Mental Retardation Smith Fineman Myers Type MNT028 SFMS
Mental Retardation Syndrome, Belgian Type MNT030
Mental Retardation Syndrome, Mietens-Weber Type MNT254
Mental Retardation with Language Impairment and with or Without Autistic Features MNT237 MRLIAF
Mental Retardation with Optic Atrophy, Deafness, and Seizures MNT308 GUST
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature MNT316
Mental Retardation with Spastic Paraplegia MNT250
Mental Retardation with Spastic Paraplegia and Palmoplantar Hyperkeratosis MNT253
Mental Retardation, Anterior Maxillary Protrusion, and Strabismus MNT118 MRAMS
Mental Retardation, Autosomal Dominant 10 MNT186 MRD10
Mental Retardation, Autosomal Dominant 11 MNT184 MRD11
Mental Retardation, Autosomal Dominant 13 MNT143 MRD13
Mental Retardation, Autosomal Dominant 18 MNT157 MRD18
Mental Retardation, Autosomal Dominant 19 MNT159 MRD19
Mental Retardation, Autosomal Dominant 20 MNT319 MRD20
Mental Retardation, Autosomal Dominant 21 MNT179 MRD21
Mental Retardation, Autosomal Dominant 22 MNT158 MRD22
Mental Retardation, Autosomal Dominant 23 MNT211 MRD23
Mental Retardation, Autosomal Dominant 24 MNT214 MRD24
Mental Retardation, Autosomal Dominant 26 MNT212 MRD26
Mental Retardation, Autosomal Dominant 27 MNT322 MRD27
Mental Retardation, Autosomal Dominant 29 MNT222 MRD29
Mental Retardation, Autosomal Dominant 30 MNT219 MRD30
Mental Retardation, Autosomal Dominant 31 MNT226 MRD31
Mental Retardation, Autosomal Dominant 32 MNT241 MRD32
Mental Retardation, Autosomal Dominant 33 MNT240 MRD33
Mental Retardation, Autosomal Dominant 34 MNT238 MRD34
Mental Retardation, Autosomal Dominant 35 MNT239 MRD35
Mental Retardation, Autosomal Dominant 36 MNT245 MRD36
Mental Retardation, Autosomal Dominant 38 MNT246 MRD38
Mental Retardation, Autosomal Dominant 39 MNT236 MRD39
Mental Retardation, Autosomal Dominant 40 MNT242 MRD40
Mental Retardation, Autosomal Dominant 41 MNT272 MRD41
Mental Retardation, Autosomal Dominant 42 MNT262 MRD42
Mental Retardation, Autosomal Dominant 43 MNT280 MRD43
Mental Retardation, Autosomal Dominant 44 MNT273 MRD44
Mental Retardation, Autosomal Dominant 45 MNT286 MRD45
Mental Retardation, Autosomal Dominant 46 MNT278 MRD46
Mental Retardation, Autosomal Dominant 47 MNT279 MRD47
Mental Retardation, Autosomal Dominant 48 MNT323 MRD48
Mental Retardation, Autosomal Dominant 49 MNT324 MRD49
Mental Retardation, Autosomal Dominant 50 MNT326 MRD50
Mental Retardation, Autosomal Dominant 51 MNT327 MRD51
Mental Retardation, Autosomal Dominant 52 MNT328 MRD52
Mental Retardation, Autosomal Dominant 53 MNT329 MRD53
Mental Retardation, Autosomal Dominant 54 MNT330 MRD54
Mental Retardation, Autosomal Dominant 55, with Seizures MNT331 MRD55
Mental Retardation, Autosomal Dominant 56 MNT332 MRD56
Mental Retardation, Autosomal Dominant 57 MNT334 MRD57
Mental Retardation, Autosomal Dominant 58 MNT337 MRD58
Mental Retardation, Autosomal Dominant 6, with or Without Seizures MNT320 MRD6
Mental Retardation, Autosomal Dominant 7 MNT185 MRD7
Mental Retardation, Autosomal Recessive 14 MNT154 MRT14
Mental Retardation, Autosomal Recessive 15 MNT150 MRT15
Mental Retardation, Autosomal Recessive 16 MNT167 MRT16
Mental Retardation, Autosomal Recessive 18 MNT151 MRT18
Mental Retardation, Autosomal Recessive 19 MNT182 MRT19
Mental Retardation, Autosomal Recessive 2 MNT155 MRT2A
Mental Retardation, Autosomal Recessive 23 MNT170 MRT23
Mental Retardation, Autosomal Recessive 24 MNT162 MRT24
Mental Retardation, Autosomal Recessive 25 MNT172 MRT25
Mental Retardation, Autosomal Recessive 27 MNT177 MRT27
Mental Retardation, Autosomal Recessive 28 MNT165 MRT28
Mental Retardation, Autosomal Recessive 29 MNT161 MRT29
Mental Retardation, Autosomal Recessive 30 MNT163 MRT30
Mental Retardation, Autosomal Recessive 31 MNT160 MRT31
Mental Retardation, Autosomal Recessive 33 MNT180 MRT33
Mental Retardation, Autosomal Recessive 34, with Variant Lissencephaly MNT283 MRT34
Mental Retardation, Autosomal Recessive 35 MNT181 MRT35
Mental Retardation, Autosomal Recessive 36 MNT183 MRT36
Mental Retardation, Autosomal Recessive 37 MNT321 MRT37
Mental Retardation, Autosomal Recessive 38 MNT176 MRT38
Mental Retardation, Autosomal Recessive 39 MNT166 MRT39
Mental Retardation, Autosomal Recessive 40 MNT213 MRT40
Mental Retardation, Autosomal Recessive 41 MNT216 MRT41
Mental Retardation, Autosomal Recessive 42 MNT210 MRT42
Mental Retardation, Autosomal Recessive 43 MNT215 MRT43
Mental Retardation, Autosomal Recessive 44 MNT221 MRT44
Mental Retardation, Autosomal Recessive 45 MNT220 MRT45
Mental Retardation, Autosomal Recessive 46 MNT227 MRT46
Mental Retardation, Autosomal Recessive 47 MNT225 MRT47
Mental Retardation, Autosomal Recessive 48 MNT234 MRT48
Mental Retardation, Autosomal Recessive 49 MNT244 MRT49
Mental Retardation, Autosomal Recessive 5 MNT145 MRT5
Mental Retardation, Autosomal Recessive 50 MNT243 MRT50
Mental Retardation, Autosomal Recessive 51 MNT263 MRT51
Mental Retardation, Autosomal Recessive 52 MNT264 MRT52
Mental Retardation, Autosomal Recessive 53 MNT270 MRT53
Mental Retardation, Autosomal Recessive 54 MNT277 MRT54
Mental Retardation, Autosomal Recessive 55 MNT282 MRT55
Mental Retardation, Autosomal Recessive 56 MNT284 MRT56
Mental Retardation, Autosomal Recessive 57 MNT287 MRT57
Mental Retardation, Autosomal Recessive 58 MNT285 MRT58
Mental Retardation, Autosomal Recessive 59 MNT281 MRT59
Mental Retardation, Autosomal Recessive 60 MNT275 MRT60
Mental Retardation, Autosomal Recessive 61 MNT325 MRT61
Mental Retardation, Autosomal Recessive 63 MNT335 MRT63
Mental Retardation, Autosomal Recessive 64 MNT336 MRT64
Mental Retardation, Autosomal Recessive 65 MNT338 MRT65
Mental Retardation, Buenos Aires Type MNT256
Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma MNT317 MEDNIK
Mental Retardation, Fra12a Type MNT107
Mental Retardation, Keratoconus, Febrile Seizures, and Sinoatrial Block MNT039
Mental Retardation, Microcephaly, Epilepsy, and Coarse Face MNT251
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism MNT315
Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies MNT259
Mental Retardation, Severe, with Spasticity and Pigmentary Tapetoretinal Degeneration MNT311 MRST
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations MNT314
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy MNT252 CHRS
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome MNT318 MORMS
Mental Retardation, X-Linked 100 MNT223 MRX100
Mental Retardation, X-Linked 101 MNT224 MRX101
Mental Retardation, X-Linked 102 MNT248 MRX102
Mental Retardation, X-Linked 103 MNT289 MRX103
Mental Retardation, X-Linked 104 MNT267 MRX104
Mental Retardation, X-Linked 105 MNT274 MRX105
Mental Retardation, X-Linked 106 MNT294 MRX106
Mental Retardation, X-Linked 107 MNT333 MRX107
Mental Retardation, X-Linked 12 MNT305 MRX12
Mental Retardation, X-Linked 21 MNT301 MRX21
Mental Retardation, X-Linked 23 MNT204 MRX23
Mental Retardation, X-Linked 42 MNT205 MRX42
Mental Retardation, X-Linked 49 MNT187 MRX49
Mental Retardation, X-Linked 50 MNT194 MRX50
Mental Retardation, X-Linked 53 MNT202 MRX53
Mental Retardation, X-Linked 73 MNT247 MRX73
Mental Retardation, X-Linked 92 MNT196 MRX92
Mental Retardation, X-Linked 96 MNT195 MRX96
Mental Retardation, X-Linked 97 MNT200 MRX97
Mental Retardation, X-Linked 98 MNT198 MRX98
Mental Retardation, X-Linked 99 MNT218 MRX99
Mental Retardation, X-Linked 99, Syndromic, Female-Restricted MNT290 MRXS99F
Mental Retardation, X-Linked, Associated with Fragile Site Fraxe MNT307 MRFRAXE
Mental Retardation, X-Linked, Syndromic 13 MNT135 MRXS13
Mental Retardation, X-Linked, Syndromic 17 MNT191
Mental Retardation, X-Linked, Syndromic 32 MNT207 MRXS32
Mental Retardation, X-Linked, Syndromic 33 MNT295 MRXS33
Mental Retardation, X-Linked, Syndromic 34 MNT296 MRXS34
Mental Retardation, X-Linked, Syndromic 9 MNT197 MRXS9
Mental Retardation, X-Linked, Syndromic, 35 MNT298 MRXS35
Mental Retardation, X-Linked, Syndromic, Bain Type MNT269 MRXSB
Mental Retardation, X-Linked, Syndromic, Cabezas Type MNT303 MRXS15
Mental Retardation, X-Linked, Syndromic, Christianson Type MNT302 MRXSCH
Mental Retardation, X-Linked, Syndromic, Chudley-Schwartz Type MNT201
Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type MNT228 MRXSCJ
Mental Retardation, X-Linked, Syndromic, Hedera Type MNT192 MRXE
Mental Retardation, X-Linked, Syndromic, Houge Type MNT306 MRXSHG
Mental Retardation, X-Linked, Syndromic, Martin-Probst Type MNT146 MRXSMP
Mental Retardation, X-Linked, Syndromic, Nascimento Type MNT056 MRXSN
Mental Retardation, X-Linked, Syndromic, Raymond Type MNT057 MRXSZ
Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type MNT310 MRXSSR
Mental Retardation, X-Linked, Syndromic, Turner Type MNT058 MRXST
Mental Retardation, X-Linked, Syndromic, Wu Type MNT258 MRX94
Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance MNT229 MRXSO
Mental Retardation, X-Linked, with Craniofacial Dysmorphism MNT257
Mental Retardation, X-Linked, with or Without Seizures, Arx-Related MNT304 MRXARX
Mental Retardation, X-Linked, with Panhypopituitarism MNT300 MRXGH
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 MNT309 MRXSHF1
Mepan Syndrome MPN002 DYT29
Mepivacaine Allergy MPV003
Meralgia Paraesthetica, Familial MRL006
Meralgia Paresthetica MRL001
Mercaptolactate-Cysteine Disulfiduria MRC009 MCDU
Mercury Poisoning MRC003
Merkel Cell Carcinoma MRK001 MCC
Merlob Grunebaum Reisner Syndrome MRL002
Meropenem Allergy MRP005
Mesangial Proliferative Glomerulonephritis MSN001
Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities MSN012
Mesangioproliferative Glomerulopathy MSN011
Mesenchymal Cell Neoplasm MSN004
Mesenchymal Chondrosarcoma MSN005
Mesenchymoma MSN006
Mesenteric Lymphadenitis MSN002
Mesenteric Vascular Occlusion MSN003
Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis MSL004
Mesoaxial Hexadactyly and Cardiac Malformation MSX002
Mesocardia MSC086
Mesocestoidiasis MSC001
Mesomelia MSM003
Mesomelia-Synostoses Syndrome MSM004
Mesomelic Dwarfism Cleft Palate Camptodactyly MSM005
Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type MSM006
Mesomelic Dysplasia Skin Dimples MSM009
Mesomelic Dysplasia, Camera Type MSM020
Mesomelic Dysplasia, Kantaputra Type MSM016 MDK
Mesomelic Dysplasia, Savarirayan Type MSM019
Mesomelic Limb Shortening and Bowing MSM018
Mesothelioma, Malignant MST023 MESOM
Metabolic Acidosis MTB004
Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration MTB007 MECRCN
Metacarpal 4-5 Fusion MTC100 MF4
Metachondromatosis MTC018 MC
Metachromasia of Fibroblasts MTC131
Metachromatic Leukodystrophy MTC003 MLD
Metachromatic Leukodystrophy Due to Saposin B Deficiency MTC019 MLD-SAPB
Metachromatic Leukodystrophy, Adult Form MTC074
Metachromatic Leukodystrophy, Adult-Onset, with Normal Arylsulfatase a MTC132
Metachromatic Leukodystrophy, Juvenile Form MTC076
Metachromatic Leukodystrophy, Late Infantile Form MTC075
Metachronous Kidney Wilms' Tumor MTC002
Metachronous Osteosarcoma of the Bone MTC001
Metagonimiasis MTG001
Metal Allergy MTL005
Metal Metabolism Disorder MTL002
Metanephric Adenoma MTN001
Metaphyseal Acroscyphodysplasia MTP004
Metaphyseal Anadysplasia MTP005 MAD
Metaphyseal Anadysplasia 2 MTP014 MANDP2
Metaphyseal Chondrodysplasia with Cone-Shaped Epiphyses, Normal Hair, and Normal Hands MTP007
Metaphyseal Chondrodysplasia, Jansen Type MTP034 JMC
Metaphyseal Chondrodysplasia, Kaitila Type MTP017
Metaphyseal Chondrodysplasia, Others MTP008
Metaphyseal Chondrodysplasia, Pena Type MTP035
Metaphyseal Chondrodysplasia, Schmid Type MTP025 SMCD
Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness MTP032
Metaphyseal Dysostosis-Intellectual Disability-Conductive Deafness Syndrome MTP027
Metaphyseal Dysplasia Maxillary Hypoplasia Brachydactyly MTP010
Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly MTP023 MDMHB
Metaphyseal Dysplasia Without Hypotrichosis MTP003 CHHV
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy MTP036
Metaphyseal Dysplasia, Braun-Tinschert Type MTP021
Metaphyseal Dysplasia, Spahr Type MTP028 MDST
Metaphyseal Enchondromatosis with D-2-Hydroxyglutaric Aciduria MTP033
Metaphyseal Modeling Abnormality, Skin Lesions, and Spastic Paraplegia MTP037
Metaphyseal Undermodeling, Spondylar Dysplasia, and Overgrowth MTP011
Metastatic Insulinoma MTS004
Metastatic Squamous Neck Cancer with Occult Primary MTS005
Metatarsus Adductus MTT004
Metatarsus Varus, Type I MTT007
Metatropic Dysplasia MTT002 MTD
Metatypical Basal Cell Carcinoma MTT001
Methane Production MTH071
Methanol Poisoning MTH047
Methemoglobin Reductase Deficiency MTH072
Methemoglobinemia MTH007
Methemoglobinemia and Ambiguous Genitalia MTH082 METAG
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase MTH026 METHB-CYB5R3
Methemoglobinemia, Alpha Type MTH084
Methemoglobinemia, Beta Type MTH083
Methemoglobinemia, Beta-Globin Type MTH064
Methimazole Antenatal Exposure MTH070
Methionine Adenosyltransferase Deficiency MTH011
Methionine Adenosyltransferase I/iii Deficiency MTH074 MATD
Methionine Malabsorption Syndrome MTH075
Methotrexate Toxicity or Dose Selection MTH061
Methotrexate-Associated Lymphoproliferation MTH001
Methotrexate-Associated Lymphoproliferative Disorders MTH049
Methyl Isocyanate Allergic Asthma MTH085
Methylcobalamin Deficiency, Cbl E Complementation Type MTH020
Methylmalonate Semialdehyde Dehydrogenase Deficiency MTH013 MMSDHD
Methylmalonic Acidemia and Homocysteinemia, Cblx Type MTH079 MRX3
Methylmalonic Acidemia Due to Transcobalamin Receptor Defect MTH069
Methylmalonic Acidemia with Homocystinuria MTH021
Methylmalonic Acidemia with Homocystinuria Type Cblj MTH067 MAHCJ
Methylmalonic Aciduria and Homocystinuria Type Cble MTH003
Methylmalonic Aciduria and Homocystinuria Type Cblg MTH002
Methylmalonic Aciduria and Homocystinuria, Cblc Type MTH054 MAHCC
Methylmalonic Aciduria and Homocystinuria, Cbld Type MTH055 MAHCD
Methylmalonic Aciduria and Homocystinuria, Cblf Type MTH056 MAHCF
Methylmalonic Aciduria and Homocystinuria, Cblj Type MTH051 MAHCJ
Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency MTH076 MMAM
Methylmalonic Aciduria Microcephaly Cataract MTH023
Methylmalonic Aciduria, Cbla Type MTH077 MMAA
Methylmalonic Aciduria, Cblb Type MTH078 MMAB
Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect MTH068 MMATC
Methylmalonyl-Coa Epimerase Deficiency MTH040 MCEED
Methylmalonyl-Coenzyme a Mutase Deficiency MTH025
Metopic Ridging-Ptosis-Facial Dysmorphism Syndrome MTP038
Mevalonic Aciduria MVL001 MEVA
Michels Caskey Syndrome MCH009
Microbrachycephaly Ptosis Cleft Lip MCR042
Microcephalic Osteodysplastic Dysplasia, Saul-Wilson Type MCR197
Microcephalic Osteodysplastic Primordial Dwarfism, Type I MCR240 MOPD
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii MCR258 MOPD2
Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii MCR331 MOPD3
Microcephalic Primordial Dwarfism, Montreal Type MCR274
Microcephalic Primordial Dwarfism, Toriello Type MCR308
Microcephalic Primordial Dwarfism-Insulin Resistance Syndrome MCR279
Microcephaly MCR010
Microcephaly 1, Primary, Autosomal Recessive MCR247 MCPH1
Microcephaly 10, Primary, Autosomal Recessive MCR223 MCPH10
Microcephaly 11, Primary, Autosomal Recessive MCR249 MCPH11
Microcephaly 12, Primary, Autosomal Recessive MCR246 MCPH12
Microcephaly 13, Primary, Autosomal Recessive MCR236 MCPH13
Microcephaly 14, Primary, Autosomal Recessive MCR270 MCPH14
Microcephaly 15, Primary, Autosomal Recessive MCR269 MCPH15
Microcephaly 16, Primary, Autosomal Recessive MCR314 MCPH16
Microcephaly 17, Primary, Autosomal Recessive MCR320 MCPH17
Microcephaly 18, Primary, Autosomal Dominant MCR322 MCPH18
Microcephaly 19, Primary, Autosomal Recessive MCR356 MCPH19
Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations MCR222 MCPH2
Microcephaly 20, Primary, Autosomal Recessive MCR360 MCPH20
Microcephaly 21, Primary, Autosomal Recessive MCR361 MCPH21
Microcephaly 22, Primary, Autosomal Recessive MCR362 MCPH22
Microcephaly 23, Primary, Autosomal Recessive MCR363 MCPH23
Microcephaly 3, Primary, Autosomal Recessive MCR248 MCPH3
Microcephaly 4, Primary, Autosomal Recessive MCR254 MCPH4
Microcephaly 5, Primary, Autosomal Recessive MCR239 MCPH5
Microcephaly 6, Primary, Autosomal Recessive MCR250 MCPH6
Microcephaly 7, Primary, Autosomal Recessive MCR238 MCPH7
Microcephaly 8, Primary, Autosomal Recessive MCR243 MCPH8
Microcephaly 9, Primary, Autosomal Recessive MCR255 MCPH9
Microcephaly and Chorioretinopathy 1 MCR282
Microcephaly and Chorioretinopathy 2 MCR283
Microcephaly and Chorioretinopathy 3 MCR284
Microcephaly and Chorioretinopathy, Autosomal Recessive, 1 MCR259 MCCRP1
Microcephaly and Chorioretinopathy, Autosomal Recessive, 2 MCR244 MCCRP2
Microcephaly and Chorioretinopathy, Autosomal Recessive, 3 MCR272 MCCRP3
Microcephaly Brain Defect Spasticity Hypernatremia MCR046
Microcephaly Chorioretinopathy Recessive Form MCR048
Microcephaly Hypergonadotropic Hypogonadism Short Stature MCR051
Microcephaly Microcornea Syndrome Seemanova Type MCR052
Microcephaly Micropenis Convulsions MCR053
Microcephaly Microphthalmos Blindness MCR054
Microcephaly Nonsyndromal MCR055
Microcephaly Pontocerebellar Hypoplasia Dyskinesia MCR056
Microcephaly with Cervical Spine Fusion Anomalies MCR305
Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia MCR309
Microcephaly with Chorioretinopathy, Autosomal Dominant Form MCR059
Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation MCR216 MCLMR
Microcephaly with Simplified Gyral Pattern MCR345
Microcephaly with Spastic Quadriplegia MCR060
Microcephaly, Amish Type MCR257 MCPHA
Microcephaly, Autosomal Dominant MCR329
Microcephaly, Cerebellar Hypoplasia, and Cardiac Conduction Defect Syndrome MCR311
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis MCR315 MCCPD
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs MCR304
Microcephaly, Corpus Callosum Dysgenesis, and Cleft Lip/palate MCR340
Microcephaly, Epilepsy, and Diabetes Syndrome MCR209 MEDS
Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation MCR344
Microcephaly, Facial Dysmorphism, Renal Agenesis, and Ambiguous Genitalia Syndrome MCR366 MFRG
Microcephaly, Growth Restriction, and Increased Sister Chromatid Exchange 2 MCR365
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance MCR351
Microcephaly, Macrotia, and Mental Retardation MCR342
Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy MCR123 MCPHSBA
Microcephaly, Progressive, with Seizures and Cerebral and Cerebellar Atrophy MCR355 MSCCA
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract MCR341
Microcephaly, Seizures, and Developmental Delay MCR064 MCSZ
Microcephaly, Seizures, Spasticity, and Brain Calcifications MCR333 MISSBC
Microcephaly, Severe, with Skeletal Anomalies Including Posterior Rib-Gap Defects MCR343
Microcephaly, Short Stature, and Impaired Glucose Metabolism 1 MCR323 MSSGM1
Microcephaly, Short Stature, and Impaired Glucose Metabolism 2 MCR316 MSSGM2
Microcephaly, Short Stature, and Limb Abnormalities MCR327 MISSLA
Microcephaly, Short Stature, and Polymicrogyria with or Without Seizures MCR354 MSSP
Microcephaly-Capillary Malformation Syndrome MCR183 MICCAP
Microcephaly-Cardiomyopathy MCR066
Microcephaly-Cleft Palate-Abnormal Retinal Pigmentation Syndrome MCR357
Microcephaly-Complex Motor and Sensory Axonal Neuropathy Syndrome MCR298
Microcephaly-Corpus Callosum and Cerebellar Vermis Hypoplasia-Facial Dysmorphism-Intellectual Disability Syndrom MCR358
Microcephaly-Deafness Syndrome MCR306
Microcephaly-Facial Dysmorphism-Ocular Anomalies-Multiple Congenital Anomalies Syndrome MCR367
Microcephaly-Intellectual Disability-Phalangeal and Neurological Anomalies Syndrome MCR286
Microcephaly-Micromelia Syndrome MCR326 MIMIS
Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome MCR285
Microcephaly-Seizures-Intellectual Disability-Heart Disease Syndrome MCR295
Microcephaly-Short Stature-Intellectual Disability-Facial Dysmorphism Syndrome MCR280
Microcolon MCR334
Microcoria, Congenital MCR067 MCOR
Microcornea Corectopia Macular Hypoplasia MCR069
Microcornea Posterior Megalolenticonus Persistent Fetal Vasculature Coloboma MCR207
Microcornea, Glaucoma, and Absent Frontal Sinuses MCR070
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus MCR220 MMCAT
Microcystic Adenoma MCR014
Microcystic Lymphatic Malformation MCR193
Microcystic Meningioma MCR001
Microcystic Variant Infiltrating Bladder Urothelial Carcinoma MCR008
Microcytic Anemia MCR018
Microdontia Hypodontia Short Stature MCR072
Microform Holoprosencephaly MCR173 HPE-L
Microgastria Limb Reduction Defect MCR073 MLRD
Microgastria-Limb Reduction Defects Association MCR310 MLRD
Microglandular Adenosis MCR019
Microglandular Adenosis of Breast MCR012
Microhydranencephaly MCR025 MHAC
Microinvasive Cervical Squamous Cell Carcinoma MCR015
Microinvasive Gastric Cancer MCR011
Microlissencephaly MCR099
Microlissencephaly-Micromelia Syndrome MCR299
Micromelic Bone Dysplasia with Cloverleaf Skull MCR074
Micronodular Basal Cell Carcinoma MCR016
Micropapillary Variant Infiltrating Bladder Urothelial Carcinoma MCR006
Micropapillomatosis Labialis MCR007
Microphthalmia MCR013
Microphthalmia Associated with Colobomatous Cyst MCR075
Microphthalmia Microtia Fetal Akinesia MCR078
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies MCR348
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies MCR336
Microphthalmia with Limb Anomalies MCR165 OAS
Microphthalmia, Isolated 1 MCR124 MCOP
Microphthalmia, Isolated 2 MCR137 MCOP2
Microphthalmia, Isolated 3 MCR114 MCOP3
Microphthalmia, Isolated 4 MCR109 MCOP4
Microphthalmia, Isolated 5 MCR122 MCOP5
Microphthalmia, Isolated 6 MCR211 MCOP6
Microphthalmia, Isolated 7 MCR108 MCOP7
Microphthalmia, Isolated 8 MCR219 MCOP8
Microphthalmia, Isolated, with Cataract 1 MCR330 CATM
Microphthalmia, Isolated, with Coloboma 1 MCR338
Microphthalmia, Isolated, with Coloboma 10 MCR271 MCOPCB10
Microphthalmia, Isolated, with Coloboma 2 MCR346
Microphthalmia, Isolated, with Coloboma 3 MCR349 MCOPCB3
Microphthalmia, Isolated, with Coloboma 4 MCR335
Microphthalmia, Isolated, with Coloboma 5 MCR350 MCOPCB5
Microphthalmia, Isolated, with Coloboma 6 MCR352 MCOPCB6
Microphthalmia, Isolated, with Coloboma 7 MCR210 MCOPCB7
Microphthalmia, Isolated, with Coloboma 9 MCR214 MCOPCB9
Microphthalmia, Isolated, with Corectopia MCR087
Microphthalmia, Syndromic 1 MCR263 MCOPS1
Microphthalmia, Syndromic 10 MCR312 MOBA
Microphthalmia, Syndromic 11 MCR217 MCOPS11
Microphthalmia, Syndromic 12 MCR212 MCOPS12
Microphthalmia, Syndromic 13 MCR228 MCOPS13
Microphthalmia, Syndromic 2 MCR261 MCOPS2
Microphthalmia, Syndromic 3 MCR241 MCOPS3
Microphthalmia, Syndromic 4 MCR262
Microphthalmia, Syndromic 5 MCR252 MCOPS5
Microphthalmia, Syndromic 6 MCR251 MCOPS6
Microphthalmia, Syndromic 8 MCR245 MCOPS8
Microphthalmia, Syndromic 9 MCR256 MCOPS9
Microphthalmia/anophthalmia/coloboma Spectrum MCR273
Microphthalmia/coloboma and Skeletal Dysplasia Syndrome MCR324 MCSKS
Microscopic Breast Papilloma MCR009
Microscopic Colitis MCR191
Microscopic Polyangiitis MCR088 MPA
Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or Without Secondary Glaucoma MCR253 MSPKA
Microspherophakia with Hernia MCR090
Microspherophakia-Metaphyseal Dysplasia MCR307
Microsporidiosis MCR020
Microtia MCR103
Microtia with Meatal Atresia and Conductive Deafness MCR337
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma MCR242
Microtia, Hearing Impairment, and Cleft Palate MCR119 MCRT
Microtia-Anotia MCR093 M-A
Microtriplication 11q24.1 MCR186
Microvascular Complications of Diabetes 1 MCR129 MVCD1
Microvascular Complications of Diabetes 2 MCR112 MVCD2
Microvascular Complications of Diabetes 3 MCR113 MVCD3
Microvascular Complications of Diabetes 4 MCR133 MVCD4
Microvascular Complications of Diabetes 5 MCR115 MVCD5
Microvascular Complications of Diabetes 6 MCR130 MVCD6
Microvascular Complications of Diabetes 7 MCR120 MVCD7
Micturation-Induced Seizures MCT004
Mid-Dermal Elastolysis MDD015
Middle Cerebral Artery Infarction MDD003
Middle Cranial Fossa Meningioma MDD001
Middle Ear Adenocarcinoma MDD004
Middle Ear Adenoma MDD008
Middle Ear Carcinoma MDD009
Middle Ear Cholesterol Granuloma MDD006
Middle Ear Disease MDD010
Middle Ear Neuroendocrine Tumor MDD017
Middle Ear Squamous Cell Carcinoma MDD007
Middle Lobe Syndrome MDD005
Midface Dysplasia MDF001
Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis MDF002 MFHIEN
Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia MDF004
Midline Cervical Cleft MDL016
Midline Cleft of Lower Lip MDL010
Midline Cystocele MDL004
Midline Interhemispheric Variant of Holoprosencephaly MDL020 MIH
Midline Malformations, Multiple, with Limb Abnormalities and Hypopituitarism MDL027
Midphalangeal Hair MDP001
Migraine with Aura MGR003
Migraine with Aura 7 MGR025 MGR7
Migraine with Aura 9 MGR027 MGR9
Migraine with Brainstem Aura MGR035 MBA
Migraine with or Without Aura 1 MGR028 MA
Migraine with or Without Aura 10 MGR038 MGR10
Migraine with or Without Aura 11 MGR039 MGR11
Migraine with or Without Aura 12 MGR040 MGR12
Migraine with or Without Aura 13 MGR042 MGR13
Migraine with or Without Aura 2 MGR036 MFTS
Migraine with or Without Aura 3 MGR022 MGR3
Migraine with or Without Aura 5 MGR024 MGR5
Migraine with or Without Aura 6 MGR033 MGR6
Migraine with or Without Aura 8 MGR037 MGR8
Migraine Without Aura MGR001
Migraine Without Aura 4 MGR023 MGOA
Migraine, Familial Hemiplegic, 1 MGR032 FHM1
Migraine, Familial Hemiplegic, 2 MGR030 FHM2
Migraine, Familial Hemiplegic, 3 MGR031 FHM3
Mikulicz Disease MKL001
Mild Hyperphenylalaninemia MLD011 MHPA
Mild Phenylketonuria MLD010 MPKU
Mild Pre-Eclampsia MLD002
Miles-Carpenter Syndrome MLS013 MCS
Milia, Multiple Eruptive MLM001 MEM
Miliaria MLR009
Miliaria Rubra MLR001
Miliary Tuberculosis MLR002
Milk Allergy MLK006
Milker's Nodule MLK001
Miller Fisher Syndrome MLL002
Miller-Dieker Lissencephaly Syndrome MLL018 MDLS
Mills Syndrome MLL015
Milner Khallouf Gibson Syndrome MLN017
Mineral Metabolism Disease MNR003
Mini Stroke MNS002
Minicore Myopathy with External Ophthalmoplegia MNC011 MMDO
Minicore Myopathy, Antenatal Onset, with Arthrogryposis MNC012
Minimal Pigment Oculocutaneous Albinism Type 1 MNM005
Minor Vestibular Glands Adenoma MNR001
Mirage Syndrome MRG013 MIRAGE
Mirizzi Syndrome MRZ001
Mirror Agnosia MRR002
Mirror Movements 1 MRR011 MRMV1
Mirror Movements 2 MRR010 MRMV2
Mirror Movements 3 MRR012 MRMV3
Mirror Polydactyly Segmentation and Limbs Defects MRR005
Mirror Polydactyly-Vertebral Segmentation-Limbs Defects Syndrome MRR013
Mismatch Repair Cancer Syndrome MSM014 MMRCS
Misophonia MSP003
Mitchell-Riley Syndrome MTC096 MTCHRS
Mite Infestation MTN002
Mitochondrial Complex I Deficiency MTC007 MT-C1D
Mitochondrial Complex I Deficiency Due to Acad9 Deficiency MTC107 ACAD9 DEFICIENCY
Mitochondrial Complex Ii Deficiency MTC020 MT-C2D
Mitochondrial Complex Iii Deficiency MTC008
Mitochondrial Complex Iii Deficiency, Nuclear Type 1 MTC085 MC3DN1
Mitochondrial Complex Iii Deficiency, Nuclear Type 2 MTC091 MC3DN2
Mitochondrial Complex Iii Deficiency, Nuclear Type 3 MTC089 MC3DN3
Mitochondrial Complex Iii Deficiency, Nuclear Type 4 MTC087 MC3DN4
Mitochondrial Complex Iii Deficiency, Nuclear Type 6 MTC090 MC3DN6
Mitochondrial Complex Iii Deficiency, Nuclear Type 7 MTC095 MC3DN7
Mitochondrial Complex Iii Deficiency, Nuclear Type 8 MTC094 MC3DN8
Mitochondrial Complex Iii Deficiency, Nuclear Type 9 MTC098 MC3DN9
Mitochondrial Complex Iv Deficiency MTC097 MT-C4D
Mitochondrial Complex V Deficiency, Nuclear Type 1 MTC029 MC5DN1
Mitochondrial Complex V Deficiency, Nuclear Type 2 MTC068 MC5DN2
Mitochondrial Complex V Deficiency, Nuclear Type 3 MTC030 MC5DN3
Mitochondrial Complex V Deficiency, Nuclear Type 4 MTC137 MC5DN4
Mitochondrial Complex V Deficiency, Nuclear Type 5 MTC141
Mitochondrial Disease with Severe Hypotonia, Lactic Acidaemia and Hyperammonemia MTC022
Mitochondrial Disorders MTC069
Mitochondrial Dna Deletion Syndromes MTC014
Mitochondrial Dna Depletion Syndrome MTC010
Mitochondrial Dna Depletion Syndrome 1 MTC061 MTDPS1
Mitochondrial Dna Depletion Syndrome 11 MTC078 MTDPS11
Mitochondrial Dna Depletion Syndrome 12a MTC142
Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant MTC139 MTDPS12A
Mitochondrial Dna Depletion Syndrome 12b MTC143
Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive MTC138 MTDPS12B
Mitochondrial Dna Depletion Syndrome 13 MTC088 MTDPS13
Mitochondrial Dna Depletion Syndrome 14 MTC126 MTDPS14
Mitochondrial Dna Depletion Syndrome 15 MTC129 MTDPS15
Mitochondrial Dna Depletion Syndrome 2 MTC062 MTDPS2
Mitochondrial Dna Depletion Syndrome 3 MTC063 MTDPS3
Mitochondrial Dna Depletion Syndrome 4a MTC056 MTDPS4A
Mitochondrial Dna Depletion Syndrome 4b MTC055 MTDPS4B
Mitochondrial Dna Depletion Syndrome 5 MTC059 MTDPS5
Mitochondrial Dna Depletion Syndrome 6 MTC058 MTDPS6
Mitochondrial Dna Depletion Syndrome 7 MTC054 MTDPS7
Mitochondrial Dna Depletion Syndrome 8a MTC065 MTDPS8A
Mitochondrial Dna Depletion Syndrome 9 MTC060 MTDPS9
Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria MTC144
Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form Due to Dguok Deficiency MTC103
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form MTC093
Mitochondrial Dna Maintenance Defects MTC140
Mitochondrial Dna-Associated Leigh Syndrome MTC112 MILS
Mitochondrial Dna-Associated Leigh Syndrome and Narp MTC015
Mitochondrial Encephalomyopathy MTC004
Mitochondrial Genetic Disorders MTC024
Mitochondrial Import-Stimulating Factor MTC135 MSF
Mitochondrial Intermembrane Space Protein Tim12, Yeast, Homolog of MTC136
Mitochondrial Membrane Protein-Associated Neurodegeneration MTC036 MPAN
Mitochondrial Metabolism Disease MTC005
Mitochondrial Myopathy MTC133
Mitochondrial Myopathy with a Defect in Mitochondrial-Protein Transport MTC134
Mitochondrial Myopathy with Diabetes MTC025
Mitochondrial Myopathy with Lactic Acidosis MTC026 MMLA
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes MTC114 MELAS
Mitochondrial Myopathy, Infantile, Transient MTC116 MMIT
Mitochondrial Myopathy, Lethal, Infantile MTC115 LIMD
Mitochondrial Neurogastrointestinal Encephalomyopathy MTC111 MNGIE
Mitochondrial Neurogastrointestinal Encephalopathy Disease MTC016 MEPOP
Mitochondrial Non-Syndromic Sensorineural Deafness MTC106
Mitochondrial Phosphate Carrier Deficiency MTC037 MPCD
Mitochondrial Pyruvate Carrier Deficiency MTC079 MPYCD
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency MTC108 ECHS1D
Mitochondrial Trifunctional Protein Deficiency MTC027 MTPD
Mitral Atresia MTR027
Mitral Valve Agenesis MTR068
Mitral Valve Disease MTR012
Mitral Valve Insufficiency MTR002
Mitral Valve Prolapse 1 MTR080 MVP1
Mitral Valve Prolapse 2 MTR077 MVP2
Mitral Valve Prolapse 3 MTR083 MVP3
Mitral Valve Prolapse, Familial, Autosomal Dominant MTR029
Mitral Valve Prolapse, Familial, X-Linked MTR030 MVP
Mitral Valve Stenosis MTR003
Miura Syndrome MRS005
Mixed Astrocytoma-Ependymoma MXD011
Mixed Astrocytoma-Ependymoma-Oligodendroglioma MXD013
Mixed Cell Adenoma MXD020
Mixed Cell Type Adenoma of Parathyroid MXD018
Mixed Cell Type Cancer MXD023
Mixed Cell Type Kidney Wilms' Tumor MXD009
Mixed Cell Uveal Melanoma MXD040
Mixed Cerebral Palsy MXD001
Mixed Connective Tissue Disease MXD005 MCTD
Mixed Cryoglobulinemia Type Iii MXD037
Mixed Cystic Lymphatic Malformation MXD041
Mixed Ductal-Endocrine Carcinoma MXD014
Mixed Endometrial Stromal and Smooth Muscle Tumor MXD017
Mixed Eosinophil-Basophil Adenoma MXD004
Mixed Epithelial Stromal Tumour MXD010
Mixed Epithelial Tumor of Ovary MXD024
Mixed Epithelial/mesenchymal Metaplastic Breast Carcinoma MXD021
Mixed Extragonadal Germ Cell Cancer MXD038
Mixed Fibrolamellar Hepatocellular Carcinoma MXD042
Mixed Germ Cell Cancer MXD025
Mixed Germ Cell Tumor MXD032
Mixed Germ Cell Tumor of Central Nervous System MXD039
Mixed Germ Cell-Sex Cord Neoplasm MXD008
Mixed Glioma MXD026
Mixed Gonadal Dysgenesis MXD016
Mixed Hepatoblastoma MXD007
Mixed Lacrimal Gland Cancer MXD003
Mixed Liposarcoma MXD006
Mixed Malaria MXD019
Mixed Mineral Dust Pneumoconiosis MXD022
Mixed Mucinous and Nonmucinous Bronchioloalveolar Adenocarcinoma MXD043
Mixed Neuroendocrine-Nonneuroendocrine Neoplasm of Pancreas MXD045
Mixed Oligodendroglioma-Astrocytoma MXD012
Mixed Receptive-Expressive Language Disorder MXD002
Mixed Sclerosing Bone Dystrophy with Extra-Skeletal Manifestations MXD034
Mixed Sleep Apnea MXD044
Mixed Type Rhabdomyosarcoma MXD015
Mixed Type Thymoma MXD027
Mixed-Type Autoimmune Hemolytic Anemia MXD035
Miyoshi Muscular Dystrophy MYS079
Miyoshi Muscular Dystrophy 1 MYS033 MMD1
Miyoshi Muscular Dystrophy 2 MYS019 MMD2
Miyoshi Muscular Dystrophy 3 MYS014 MMD3
Mobitz Type Ii Atrioventricular Block MBT001
Moderate and Severe Traumatic Brain Injury MDR006
Moderately-Differentiated Thymic Neuroendocrine Carcinoma MDR005
Modifier, X-Linked, for Neurofunctional Defects MDF003
Moebius Axonal Neuropathy Hypogonadism MBS003
Moebius Syndrome MBS002 MBS
Moebius Syndrome-Axonal Neuropathy-Hypogonadotropic Hypogonadism Syndrome MBS006
Mohr Syndrome MHR002 OFD2
Mohr-Tranebjaerg Syndrome MHR001 MTS
Mollaret Meningitis MLL006
Molluscum Contagiosum MLL001
Moloney Syndrome MLN018
Molybdenum Cofactor Deficiency MLY001 MOCOD
Molybdenum Cofactor Deficiency, Complementation Group a MLY008 MOCODA
Molybdenum Cofactor Deficiency, Complementation Group B MLY009 MOCODB
Molybdenum Cofactor Deficiency, Complementation Group C MLY010 MOCODC
Momo Syndrome MMS001
Monckeberg Arteriosclerosis MNC003
Mondini Dysplasia MND005
Mondor Disease MND006
Mongolian Spot MNG001
Monieziasis MNZ001
Monilethrix MNL001 MNLIX
Monkeypox MNK002
Monocarboxylate Transporter 1 Deficiency MNC019 MCT1D
Monoclonal Gammopathy of Uncertain Significance MNC006 MGUS
Monoclonal Mast Cell Activation Syndrome MNC020 MMAS
Monoclonal Paraproteinemia MNC004
Monocular Esotropia MNC001
Monocular Exotropia MNC005
Monocyte Chemotactic Disorder MNC021
Monocytic Leukemia MNC007
Monofixation Syndrome MNF001
Monogenic Diabetes MNG006
Mononeuritis Multiplex MNN002
Mononeuritis of Lower Limb MNN015
Mononeuritis of Upper Limb MNN003
Mononeuritis of Upper Limb and Mononeuritis Multiplex MNN016
Mononeuropathy MNN017
Mononeuropathy of the Median Nerve, Mild MNN028 MNMN
Monophalangy of Great Toe MNP012
Monophasic Synovial Sarcoma MNP001
Monosodium Glutamate Sensitivity MNS015
Monosomy 13q34 MNS013
Monosomy 21 MNS008
Monosomy 22 MNS014
Monosomy 7 of Bone Marrow MNS016 MLSM7
Monosomy 9q22.3 MNS011
Monostotic Fibrous Dysplasia MNS012
Montefiore Syndrome MNT045
Mood Disorder MDD011
Mooren's Ulcer MRN002
Morbid Obesity MRB003
Morbid Obesity and Spermatogenic Failure MRB006 MOSPGF
Morel's Ear MRL003
Morgagni Cataract MRG001
Morgellons MRG007
Morpheaform Basal Cell Carcinoma MRP002
Morphine Dependence MRP001
Morquio Syndrome MRQ003
Morquio Syndrome C MRQ002
Morse-Rawnsley-Sargent Syndrome MRS006
Morvan's Fibrillary Chorea MRV001
Mosaic Genome-Wide Paternal Uniparental Disomy MSC084
Mosaic Monosomy 18 MSC013
Mosaic Monosomy 22 MSC014
Mosaic Monosomy X MSC089
Mosaic Trisomy 1 MSC079
Mosaic Trisomy 12 MSC080
Mosaic Trisomy 13 MSC015
Mosaic Trisomy 14 MSC016
Mosaic Trisomy 15 MSC081
Mosaic Trisomy 17 MSC078
Mosaic Trisomy 22 MSC017
Mosaic Trisomy 3 MSC090
Mosaic Trisomy 4 MSC087
Mosaic Trisomy 5 MSC088
Mosaic Trisomy 6 MSC018
Mosaic Trisomy 7 MSC019
Mosaic Trisomy 8 MSC020
Mosaic Trisomy 9 MSC021
Mosaic Variegated Aneuploidy Syndrome MSC022
Mosaic Variegated Aneuploidy Syndrome 1 MSC109 MVA1
Mosaic Variegated Aneuploidy Syndrome 2 MSC106 MVA2
Mosaic Variegated Aneuploidy Syndrome 3 MSC139 MVA3
Motility-Related Diarrhea MTL001
Motion Sickness MTN003
Motor Neuron Disease MTR014
Motor Neuron Disease with Dementia and Ophthalmoplegia MTR081
Motor Neuro-Ophthalmic Disorders MTR031
Motor Neuropathy, Peripheral, with Dysautonomia MTR078
Motor Peripheral Neuropathy MTR007 HSMN
Motor Sensory Neuropathy Type 1 Aplasia Cutis Congenita MTR033
Mounier-Kuhn Syndrome MNR004
Mousa Al Din Al Nassar Syndrome MSL002
Mouth Disease MTH009
Movement Disease MVM001
Mowat-Wilson Syndrome MWT001 MOWS
Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation MWT004
Mowat-Wilson Syndrome Due to Monosomy 2q22 MWT002
Moyamoya Disease 1 MYM013 MYMY
Moyamoya Disease 2 MYM004 MYMY2
Moyamoya Disease 3 MYM005 MYMY3
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism MYM012 MYMY4
Moyamoya Disease 5 MYM003 MYMY5
Moyamoya Disease 6 with or Without Achalasia MYM015 MYMY6
Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome MPV001 NN
Mpv17-Related Mitochondrial Dna Maintenance Defect MPV002
Mseleni Joint Disease MSL005
Mt-Atp6-Related Mitochondrial Spastic Paraplegia MTT008
Mthfr Gene Variant MTH081
Mu Chain Disease MCH003
Mucinoses MCN011
Mucinous Adenocarcinoma MCN001
Mucinous Adenocarcinoma of Ovary MCN019
Mucinous Adenocarcinoma of the Appendix MCN018
Mucinous Adenofibroma MCN006
Mucinous Bronchioloalveolar Adenocarcinoma MCN021
Mucinous Cystadenocarcinoma MCN008
Mucinous Cystadenocarcinoma of the Pancreas MCN022
Mucinous Cystadenofibroma MCN010
Mucinous Intrahepatic Cholangiocarcinoma MCN005
Mucinous Lung Adenocarcinoma MCN023
Mucinous Ovarian Cystadenoma MCN003
Mucinous Stomach Adenocarcinoma MCN009
Mucinous Tubular and Spindle Renal Cell Carcinoma MCN004
Mucin-Rich Endometrial Endometrioid Adenocarcinoma MCN002
Muckle-Wells Syndrome MCK007 MWS
Mucocele of Appendix MCC004
Mucocele of Salivary Gland MCC003
Mucocutaneous Leishmaniasis MCC002
Mucoepidermoid Carcinoma MCP006 MEC
Mucoepidermoid Esophageal Carcinoma MCP008
Mucoepidermoid Thyroid Carcinoma MCP007
Mucoepithelial Dysplasia, Hereditary MCP039 HMD
Mucolipidoses MCL022
Mucolipidosis Ii Alpha/beta MCL062 MLII
Mucolipidosis Iii Alpha/beta MCL046 MLIIIA
Mucolipidosis Iii Gamma MCL016 MLIIIC
Mucolipidosis Iv MCL013 ML4
Mucopolysaccharidoses MCP033
Mucopolysaccharidoses, Unclassified Types MCP042
Mucopolysaccharidosis Iii MCP001 MPS3
Mucopolysaccharidosis Iv MCP004 MPS4
Mucopolysaccharidosis Type 2, Attenuated Form MCP034
Mucopolysaccharidosis Type 2, Severe Form MCP035
Mucopolysaccharidosis Type 6, Rapidly Progressing MCP029
Mucopolysaccharidosis Type 6, Slowly Progressing MCP028
Mucopolysaccharidosis, Type Ii MCP050 MPS2
Mucopolysaccharidosis, Type Iiia MCP043 MPS3A
Mucopolysaccharidosis, Type Iiib MCP044 MPS3B
Mucopolysaccharidosis, Type Iiic MCP045 MPS3C
Mucopolysaccharidosis, Type Iiid MCP046 MPS3D
Mucopolysaccharidosis, Type Iva MCP047 MPS4A
Mucopolysaccharidosis, Type Ivb MCP048 MPS4B
Mucopolysaccharidosis, Type Ix MCP051 MPS9
Mucopolysaccharidosis, Type Vi MCP052 MPS6
Mucopolysaccharidosis, Type Vii MCP049 MPS7
Mucopolysaccharidosis-Plus Syndrome MCP040 MPSPS
Mucormycosis MCR141
Mucosal Melanoma MCS004
Mucositis MCS002
Mucus Inspissation of Respiratory Tract MCS005
Muenke Syndrome MNK003 MNKS
Muir-Torre Syndrome MRT001 MRTES
Mulchandani-Bhoj-Conlin Syndrome MLC004 MBCS
Mulibrey Nanism MLB001 MUL
Muller Barth Menger Syndrome MLL007
Mullerian Aplasia MLL009
Mullerian Aplasia and Hyperandrogenism MLL011 MULLAPL
Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly MLL022
Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies MLL021 MURCS
Multicentric Carpotarsal Osteolysis Syndrome MLT092 MCTO
Multicentric Castleman Disease MLT113 MCD
Multicentric Osteolysis Nephropathy MLT033
Multicentric Osteolysis, Nodulosis, and Arthropathy MLT065 MONA
Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum MLT138
Multicentric Papillary Thyroid Carcinoma MLT005
Multicentric Reticulohistiocytosis MLT016
Multicore Myopathy with Mental Retardation, Short Stature, and Hypogonadotropic Hypogonadism MLT146
Multicystic Dysplastic Kidney MLT084 MCDK
Multidrug-Resistant Tuberculosis MLT006
Multifocal Atrial Tachycardia MLT131 MAT
Multifocal Choroiditis MLT035
Multifocal Dystonia MLT132
Multifocal Lymphangioendotheliomatosis with Thrombocytopenia MLT037 MLT
Multifocal Motor Neuropathy MLT075 MMN
Multifocal Osteogenic Sarcoma MLT017
Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus MLT117
Multilocular Clear Cell Renal Cell Carcinoma MLT003
Multilocular Cystic Renal Neoplasm of Low Malignant Potential MLT165 MCRCC
Multiloculated Renal Cyst MLT112
Multiminicore Disease MLT028 MMD
Multinodular Goiter MLT008
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly MLT161 MARCH
Multiple Acyl-Coa Dehydrogenase Deficiency MLT118 GA2A
Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type MLT154
Multiple Acyl-Coa Dehydrogenase Deficiency, Severe Neonatal Type MLT155
Multiple Benign Circumferential Skin Creases on Limbs MLT104 CCSF
Multiple Carboxylase Deficiency MLT018 MCD
Multiple Chemical Sensitivity MLT001
Multiple Congenital Anomalies Syndrome with Cloverleaf Skull MLT147
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome MLT140
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1 MLT126 MCAHS1
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 MLT128 MCAHS2
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 MLT127 MCAHS3
Multiple Cranial Nerve Palsy MLT009
Multiple Enchondromatosis, Maffucci Type MLT145
Multiple Endocrine Neoplasia MLT074 MEA
Multiple Endocrine Neoplasia, Type I MLT156 MEN1
Multiple Endocrine Neoplasia, Type Iia MLT160 MEN2A
Multiple Endocrine Neoplasia, Type Iib MLT159 MEN2B
Multiple Endocrine Neoplasia, Type Iv MLT086 MEN4
Multiple Epiphyseal Dysplasia MLT007 EDM
Multiple Epiphyseal Dysplasia Due to Collagen 9 Anomaly MLT141
Multiple Epiphyseal Dysplasia with Robin Phenotype MLT144
Multiple Epiphyseal Dysplasia, Autosomal Dominant MLT142
Multiple Epiphyseal Dysplasia, Recessive MLT031 EDM4
Multiple Exostoses with Spastic Tetraparesis MLT158
Multiple Familial Trichoepithelioma MLT048 EAC
Multiple Fibroadenomas of the Breast MLT120 MFAB
Multiple Fibrofolliculoma Familial MLT051
Multiple Joint Dislocations Metaphyseal Dysplasia MLT052
Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects MLT162 JDSCD
Multiple Mitochondrial Dysfunctions Syndrome MLT027 MMDS
Multiple Mitochondrial Dysfunctions Syndrome 1 MLT068 MMDS1
Multiple Mitochondrial Dysfunctions Syndrome 2 MLT069
Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia MLT150 MMDS2
Multiple Mitochondrial Dysfunctions Syndrome 3 MLT119 MMDS3
Multiple Mitochondrial Dysfunctions Syndrome 4 MLT139 MMDS4
Multiple Mitochondrial Dysfunctions Syndrome 5 MLT151 MMDS5
Multiple Mitochondrial Dysfunctions Syndrome 6 MLT167 MMDS6
Multiple Mucosal Neuroma MLT011
Multiple Paragangliomas Associated with Polycythemia MLT106
Multiple Personality Disorder MLT010
Multiple Pterygium Syndrome, Escobar Variant MLT163 EVMPS
Multiple Pterygium Syndrome, Lethal Type MLT134 LMPS
Multiple Pterygium Syndrome, X-Linked MLT148
Multiple Respiratory Chain Enzyme Deficiencies MLT057
Multiple Sclerosis MLT020 MS
Multiple Sclerosis 2 MLT093 MS2
Multiple Sclerosis 3 MLT094 MS3
Multiple Sclerosis 4 MLT095 MS4
Multiple Sclerosis 5 MLT124 MS5
Multiple Sclerosis-Ichthyosis-Factor Viii Deficiency Syndrome MLT143
Multiple Self-Healing Squamous Epithelioma MLT152 MSSE
Multiple Skull Base Meningioma MLT004
Multiple Spinal Canal and Spinal Cord Meningioma MLT014
Multiple Sulfatase Deficiency MLT135 MSD
Multiple Synostoses Syndrome MLT072
Multiple Synostoses Syndrome 1 MLT059 SYNS1
Multiple Synostoses Syndrome 2 MLT060 SYNS2
Multiple Synostoses Syndrome 3 MLT078 SYNS3
Multiple Synostoses Syndrome 4 MLT166 SYNS4
Multiple System Atrophy 1 MLT157 MSA1
Multiple System Atrophy with Orthostatic Hypotension MLT076
Multiple System Atrophy, Cerebellar Type MLT105 MSA-C
Multiple System Atrophy, Parkinsonian Type MLT116 MSA-P
Multisystemic Smooth Muscle Dysfunction Syndrome MLT073 MSMDYS
Mumps MMP001 MUMPS
Munchausen by Proxy MNC002
Mungan Syndrome MNG003 MGS
Murcs Association MRC004
Murray Valley Encephalitis MRR003
Muscle Cancer MSC072
Muscle Cramps, Familial MSC143
Muscle Disorders MSC033
Muscle Eye Brain Disease MSC077 MEB
Muscle Hypertrophy MSC007 MSLHP
Muscle Strength Quantitative Trait Locus 1 MSC054
Muscle Tissue Disease MSC004
Muscular Atrophy MSC003
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus MSC133
Muscular Atrophy, Malignant Neurogenic MSC144
Muscular Disease MSC190
Muscular Dystrophy MSC005
Muscular Dystrophy Limb Girdle Type 2a, Erb Type MSC025
Muscular Dystrophy White Matter Spongiosis MSC026
Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy MSC149
Muscular Dystrophy, Autosomal Recessive, with Cardiomyopathy and Triangular Tongue MSC185 LGMD2W
Muscular Dystrophy, Barnes Type MSC145
Muscular Dystrophy, Becker Type MSC152 BMD
Muscular Dystrophy, Cardiac Type MSC153
Muscular Dystrophy, Congenital Merosin-Deficient, 1a MSC162 MDC1A
Muscular Dystrophy, Congenital, 1b MSC050
Muscular Dystrophy, Congenital, Davignon-Chauveau Type MSC141 MDCDC
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency MSC164 MDCI
Muscular Dystrophy, Congenital, Lmna-Related MSC165 MDCL
Muscular Dystrophy, Congenital, Megaconial Type MSC028 MDCMC
Muscular Dystrophy, Congenital, Merosin-Positive MSC029
Muscular Dystrophy, Congenital, Producing Arthrogryposis MSC131
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability MSC142 MDCCAID
Muscular Dystrophy, Congenital, with Cerebellar Atrophy MSC160
Muscular Dystrophy, Congenital, with Infantile Cataract and Hypogonadism MSC132
Muscular Dystrophy, Congenital, with Rapid Progression MSC150
Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers MSC159
Muscular Dystrophy, Duchenne and Becker Type MSC012 DBMD
Muscular Dystrophy, Duchenne Type MSC157 DMD
Muscular Dystrophy, Hemizygous Lethal Type MSC154
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 MSC175 LGMD1E
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2 MSC178 LGMD1F
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 MSC180 LGMD1G
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 4 MSC187
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 MSC169 LGMD2A
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 MSC179 LGMD2J
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 12 MSC181 LGMD2L
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 17 MSC183 LGMD2Q
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 18 MSC184 LGMD2S
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 MSC170 LGMD2B
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 21 MSC186 LGMD2Z
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 23 MSC189
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 MSC177 LGMD2D
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 MSC176 LGMD2E
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 MSC171 LGMD2C
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 MSC173 LGMD2F
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7 MSC174 LGMD2G
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 MSC172 LGMD2H
Muscular Dystrophy, Limb-Girdle, Type 1h MSC058
Muscular Dystrophy, Mabry Type MSC155
Muscular Dystrophy, Progressive Pectorodorsal MSC156
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries MSC146
Muscular Dystrophy, Scapulohumeral MSC158
Muscular Dystrophy-Dystroglycanopathy MSC002
Muscular Dystrophy-Dystroglycanopathy , Type a, 1 MSC047 MDDGA1
Muscular Dystrophy-Dystroglycanopathy , Type a, 10 MSC107 MDDGA10
Muscular Dystrophy-Dystroglycanopathy , Type a, 11 MSC167 MDDGA11
Muscular Dystrophy-Dystroglycanopathy , Type a, 12 MSC102 MDDGA12
Muscular Dystrophy-Dystroglycanopathy , Type a, 13 MSC105 MDDGA13
Muscular Dystrophy-Dystroglycanopathy , Type a, 14 MSC097 MDDGA14
Muscular Dystrophy-Dystroglycanopathy , Type a, 2 MSC043 MDDGA2
Muscular Dystrophy-Dystroglycanopathy , Type a, 3 MSC045 MDDGA3
Muscular Dystrophy-Dystroglycanopathy , Type a, 4 MSC037 MDDGA4
Muscular Dystrophy-Dystroglycanopathy , Type a, 5 MSC034 MDDGA5
Muscular Dystrophy-Dystroglycanopathy , Type a, 6 MSC041 MDDGA6
Muscular Dystrophy-Dystroglycanopathy , Type a, 7 MSC101 MDDGA7
Muscular Dystrophy-Dystroglycanopathy , Type a, 8 MSC166 MDDGA8
Muscular Dystrophy-Dystroglycanopathy , Type a, 9 MSC127 MDDGA9
Muscular Dystrophy-Dystroglycanopathy , Type B, 1 MSC048 MDDGB1
Muscular Dystrophy-Dystroglycanopathy , Type B, 14 MSC099 MDDGB14
Muscular Dystrophy-Dystroglycanopathy , Type B, 2 MSC044 MDDGB2
Muscular Dystrophy-Dystroglycanopathy , Type B, 3 MSC046 MDDGB3
Muscular Dystrophy-Dystroglycanopathy , Type B, 4 MSC038 MDDGB4
Muscular Dystrophy-Dystroglycanopathy , Type B, 5 MSC035 MDDGB5
Muscular Dystrophy-Dystroglycanopathy , Type B, 6 MSC042 MDDGB6
Muscular Dystrophy-Dystroglycanopathy , Type C, 1 MSC104 MDDGC1
Muscular Dystrophy-Dystroglycanopathy , Type C, 12 MSC118 MDDGC12
Muscular Dystrophy-Dystroglycanopathy , Type C, 14 MSC098 MDDGC14
Muscular Dystrophy-Dystroglycanopathy , Type C, 15 MSC182 CDG1O
Muscular Dystrophy-Dystroglycanopathy , Type C, 2 MSC108 MDDGC2
Muscular Dystrophy-Dystroglycanopathy , Type C, 3 MSC093 MDDGC3
Muscular Dystrophy-Dystroglycanopathy , Type C, 4 MSC103 MDDGC4
Muscular Dystrophy-Dystroglycanopathy , Type C, 5 MSC036 MDDGC5
Muscular Dystrophy-Dystroglycanopathy , Type C, 7 MSC111 MDDGC7
Muscular Dystrophy-Dystroglycanopathy , Type C, 8 MSC188
Muscular Dystrophy-Dystroglycanopathy , Type C, 9 MSC100 MDDGC9
Muscular Fibrosis Multifocal Obstructed Vessels MSC030
Muscular Hypertonia, Lethal MSC151
Muscular Hypertrophy-Hepatomegaly-Polyhydramnios Syndrome MSC130
Muscular Hypoplasia, Congenital Universal, of Krabbe MSC147
Muscular Phosphorylase Kinase Deficiency MSC031
Muscular Pseudohypertrophy-Hypothyroidism Syndrome MSC129
Musculocontractural Ehlers-Danlos Syndrome MSC134 MCEDS
Mushroom Workers' Lung MSH001
Musical Aptitude Quantitative Trait Locus MSC163
Musical Perfect Pitch MSC148 AP
Musk, Inability to Smell MSK002
Mutagen Sensitivity MTG002
Mutism MTS001
Mutyh-Associated Polyposis MTY001
Myalgia-Eosinophilia Syndrome Associated with Tryptophan MYL051
Myasthenia Gravis MYS003 MG
Myasthenia Gravis Congenital MYS011
Myasthenia Gravis with Thymus Hyperplasia MYS007 MYAS1
Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors MYS072
Myasthenia, Limb-Girdle, Autoimmune MYS071
Myasthenic Syndrome, Congenital, 10 MYS052 CMS10
Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency MYS057 CMS11
Myasthenic Syndrome, Congenital, 12 MYS074 CMS12
Myasthenic Syndrome, Congenital, 13 MYS075 CMS13
Myasthenic Syndrome, Congenital, 14 MYS078 CMS14
Myasthenic Syndrome, Congenital, 15 MYS077 CMS15
Myasthenic Syndrome, Congenital, 16 MYS064 CMS16
Myasthenic Syndrome, Congenital, 17 MYS056 CMS17
Myasthenic Syndrome, Congenital, 18 MYS065 CMS18
Myasthenic Syndrome, Congenital, 19 MYS070 CMS19
Myasthenic Syndrome, Congenital, 1a, Slow-Channel MYS046 CMS1A
Myasthenic Syndrome, Congenital, 1b, Fast-Channel MYS047 CMS1B
Myasthenic Syndrome, Congenital, 20, Presynaptic MYS068 CMS20
Myasthenic Syndrome, Congenital, 21, Presynaptic MYS069 CMS21
Myasthenic Syndrome, Congenital, 22 MYS067 CMS22
Myasthenic Syndrome, Congenital, 2a, Slow-Channel MYS062 CMS2A
Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency MYS063 CMS2C
Myasthenic Syndrome, Congenital, 3a, Slow-Channel MYS048 CMS3A
Myasthenic Syndrome, Congenital, 3b, Fast-Channel MYS049 CMS3B
Myasthenic Syndrome, Congenital, 3c, Associated with Acetylcholine Receptor Deficiency MYS050 CMS3C
Myasthenic Syndrome, Congenital, 4a, Slow-Channel MYS059 CMS4A
Myasthenic Syndrome, Congenital, 4b, Fast-Channel MYS060 CMS4B
Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency MYS061 CMS4C
Myasthenic Syndrome, Congenital, 5 MYS051 CMS5
Myasthenic Syndrome, Congenital, 6, Presynaptic MYS055 CMS6
Myasthenic Syndrome, Congenital, 7, Presynaptic MYS044 CMS7
Myasthenic Syndrome, Congenital, 8 MYS076 CMS8
Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency MYS054 CMS9
Mybpc1-Related Autosomal Recessive Non-Lethal Arthrogryposis Multiplex Congenita Syndrome MYB004
Mycetoma MYC012
Mycobacterium Abscessus MYC013
Mycobacterium Avium Complex Infections MYC088 MAI
Mycobacterium Chelonae MYC014
Mycobacterium Fortuitum MYC015
Mycobacterium Gordonae MYC016
Mycobacterium Kansasii MYC017
Mycobacterium Malmoense MYC018
Mycobacterium Marinum MYC019
Mycobacterium Tuberculosis 1 MYC084 TB
Mycobacterium Tuberculosis 2 MYC054 MTBS2
Mycobacterium Tuberculosis 3 MYC055 MTBS3
Mycobacterium Tuberculosis X-Linked MYC081 MTBSX
Mycobacterium Tuberculosis, Susceptibility to Infection by MYC020
Mycobacterium Xenopi MYC021
Mycophenolate Mofetil Embryopathy MYC060
Mycoplasma Encephalitis MYC062
Mycoplasma Pneumoniae Pneumonia MYC087
Mycosis Fungoides MYC006 MF
Mycotic Corneal Ulcer MYC004
Myd88 Deficiency MYD002 MYD88D
Mydriasis, Congenital MYD004
Mydriatic Response to Pharmacologic Agents MYD003
Myelinated Optic Nerve Fibers MYL068
Myelinoclastic Diffuse Sclerosis MYL024
Myelitis MYL001
Myelocystocele MYL044
Myelocytic Leukemia-Like Syndrome, Familial, Chronic MYL018
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay MYL073
Myelodysplastic Myeloproliferative Cancer MYL004
Myelodysplastic Syndrome MYL009 MDS
Myelodysplastic Syndrome with Excess Blasts MYL074 RAEB
Myelofibrosis MYL005 MYELOF
Myeloid and Lymphoid Neoplasms Associated with Fgfr1 Abnormalities MYL062
Myeloid and Lymphoid Neoplasms Associated with Pdgfra Rearrangement MYL060
Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 MYL059
Myeloid Leukemia MYL006
Myeloid Neoplasms Associated with Pdgfrb Rearrangement MYL061
Myeloid Proliferations Related to Down Syndrome MYL053
Myeloid Sarcoma MYL003
Myeloid Splenomegaly MYL019
Myeloid/lymphoid Neoplasm Associated with Pdgfra Rearrangement MYL066
Myeloid/lymphoid Neoplasm Associated with Pdgfrb Rearrangement MYL065
Myelolymphatic Insufficiency MYL071
Myeloma, Multiple MYL069 MM
Myelomeningocele MYL020
Myelopathy, Htlv-1-Associated MYL057 HAM
Myeloperoxidase Deficiency MYL013 MPOD
Myelophthisic Anemia MYL002
Myeloproliferative Disease, Autosomal Recessive MYL070
Myeloproliferative Disorder, Chronic, with Eosinophilia MYL067 MPE
Myeloproliferative Neoplasm MYL031 CMPD
Myeloproliferative Syndrome, Transient MYL058 MST
Myeloproliferative/lymphoproliferative Neoplasms, Familial MYL064 MPLPF
Myh-9 Related Disease MYH015
Myh9 Related Thrombocytopenia MYH004
Myhre Syndrome MYH012 MYHRS
Myiasis MYS004
Myo5b-Related Progressive Familial Intrahepatic Cholestasis MY5001
Myoblastoma MYB001
Myocardial Infarction MYC007 MCI1
Myocardial Infarction 2 MYC058 MCI2
Myocardial Stunning MYC005
Myocarditis MYC008
Myocardium Cancer MYC003
Myoclonic Cerebellar Dyssynergia MYC001
Myoclonic Encephalopathy of Infants MYC032
Myoclonic Epilepsy Associated with Ragged-Red Fibers MYC072 MERRF
Myoclonic Epilepsy in Non-Progressive Encephalopathies MYC061
Myoclonic Epilepsy Myopathy Sensory Ataxia MYC030 SCAE
Myoclonic Epilepsy of Infancy MYC068
Myoclonic Epilepsy of Lafora MYC079 EPM2
Myoclonic Epilepsy of Unverricht and Lundborg MYC080 EPM1
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders MYC082
Myoclonic Epilepsy, Familial Infantile MYC083 FIME
Myoclonic Epilepsy, Hartung Type MYC077
Myoclonic Epilepsy, Juvenile 3 MYC085 EJM3
Myoclonic Epilepsy, Juvenile 4 MYC086 EJM4
Myoclonic-Astastic Epilepsy MYC069 MAE
Myoclonic-Atonic Epilepsy MYC071 MAE
Myoclonus MYC033
Myoclonus and Ataxia MYC078
Myoclonus Epilepsy MYC026
Myoclonus Epilepsy Partial Seizure MYC027
Myoclonus, Cerebellar Ataxia, and Deafness MYC074
Myoclonus, Familial Cortical MYC066 FCM
Myoclonus, Intractable, Neonatal MYC075 NEIMY
Myoepithelioma MYP001
Myofascial Pain Syndrome MYF002
Myofibrillar Lysis MYF004
Myofibrillar Myopathy MYF003
Myofibroma MYF001
Myofibromatosis, Infantile, 1 MYF007 IMF1
Myofibromatosis, Infantile, 2 MYF010 IMF2
Myoglobinuria MYG005
Myoglobinuria Dominant Form MYG002
Myoglobinuria, Acute Recurrent, Autosomal Recessive MYG004 ARARM
Myoglobinuria, Autosomal Dominant MYG006
Myoglobinuria, Recurrent MYG007 RM-MT
Myokymia with Neonatal Epilepsy MYK001
Myoma MYM001 MYOMA
Myopathic Intestinal Pseudoobstruction MYP066
Myopathy MYP004
Myopathy - Thyrotoxic MYP026
Myopathy Due to Malate-Aspartate Shuttle Defect MYP129
Myopathy Due to Myoadenylate Deaminase Deficiency MYP071 MMDD
Myopathy Mitochondrial Cataract MYP014
Myopathy of Extraocular Muscle MYP005
Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme MYP025 HML
Myopathy with Deficiency of Iscu MYP009
Myopathy with Extrapyramidal Signs MYP086 MPXPS
Myopathy with Giant Abnormal Mitochondria MYP130
Myopathy with Hexagonally Cross-Linked Tubular Arrays MYP061
Myopathy with Lactic Acidosis, Hereditary MYP097 MEIS
Myopathy with Storage of Glycoproteins and Glycosaminoglycans MYP126
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset MYP093 EMARDD
Myopathy, Autophagic Vacuolar, Infantile-Onset MYP142
Myopathy, Autosomal Recessive, with Rigid Spine and Distal Joint Contractures MYP152 LGMD2Y
Myopathy, Centronuclear, 1 MYP123 CNM1
Myopathy, Centronuclear, 2 MYP131 CNM2
Myopathy, Centronuclear, 3 MYP096 CNM3
Myopathy, Centronuclear, 4 MYP098 CNM4
Myopathy, Centronuclear, 5 MYP148 CNM5
Myopathy, Centronuclear, 6, with Fiber-Type Disproportion MYP150 CNM6
Myopathy, Centronuclear, X-Linked MYP136 CNMX
Myopathy, Congenital MYP132
Myopathy, Congenital, Bailey-Bloch MYP151 NAM
Myopathy, Congenital, Compton-North MYP038 MYPCN
Myopathy, Congenital, with Fiber-Type Disproportion MYP091 CFTD
Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked MYP039 CFTDX
Myopathy, Distal, 1 MYP125 MPD1
Myopathy, Distal, 3 MYP112 MPD3
Myopathy, Distal, 4 MYP095 MPD4
Myopathy, Distal, 5 MYP116 MPD5
Myopathy, Distal, Infantile-Onset MYP124
Myopathy, Distal, Tateyama Type MYP067 MPDT
Myopathy, Distal, with Anterior Tibial Onset MYP035 DMAT
Myopathy, Distal, with Early Respiratory Failure, Autosomal Dominant MYP113
Myopathy, Distal, with Rimmed Vacuoles MYP120 DMRV
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia MYP128
Myopathy, Isolated Mitochondrial, Autosomal Dominant MYP099 IMMD
Myopathy, Lactic Acidosis, and Sideroblastic Anemia MYP108
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 MYP021 MLASA1
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 MYP022 MLASA2
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 MYP107 MLASA3
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay MYP017 MPMCHD
Myopathy, Mitochondrial, and Ataxia MYP149 MMYAT
Myopathy, Myofibrillar, 1 MYP072 MFM1
Myopathy, Myofibrillar, 2 MYP082 MFM2
Myopathy, Myofibrillar, 3 MYP078 MFM3
Myopathy, Myofibrillar, 4 MYP080 MFM4
Myopathy, Myofibrillar, 5 MYP079 MFM5
Myopathy, Myofibrillar, 6 MYP081 MFM6
Myopathy, Myofibrillar, 7 MYP119 MFM7
Myopathy, Myofibrillar, 8 MYP118 MFM8
Myopathy, Myofibrillar, Fatal Infantile Hypertonic, Alpha-B Crystallin-Related MYP121 MFMFIH-CRYAB
Myopathy, Myosin Storage, Autosomal Dominant MYP105 MSMA
Myopathy, Myosin Storage, Autosomal Recessive MYP106 MSMB
Myopathy, Proximal, and Ophthalmoplegia MYP139 MYPOP
Myopathy, Scapulohumeroperoneal MYP114 SHPM
Myopathy, Spheroid Body MYP094 SBM
Myopathy, Tubular Aggregate, 1 MYP087 TAM1
Myopathy, Tubular Aggregate, 2 MYP088 TAM2
Myopathy, Vacuolar, with Casq1 Aggregates MYP104 VMCQA
Myopathy, X-Linked, with Excessive Autophagy MYP100 MEAX
Myopathy, X-Linked, with Postural Muscle Atrophy MYP056 XMPMA
Myopathy-Growth Delay-Intellectual Disability-Hypospadias Syndrome MYP110
Myopericytoma MYP064
Myopia MYP006
Myopia 1, X-Linked MYP137 MYP1
Myopia 10 MYP044 MYP10
Myopia 11, Autosomal Dominant MYP143 MYP11
Myopia 12, Autosomal Dominant MYP144 MYP12
Myopia 13, X-Linked MYP134 MYP13
Myopia 14 MYP069 MYP14
Myopia 15, Autosomal Dominant MYP146 MYP15
Myopia 16, Autosomal Dominant MYP145 MYP16
Myopia 17, Autosomal Dominant MYP140 MYP17
Myopia 18, Autosomal Recessive MYP133 MYP18
Myopia 19, Autosomal Dominant MYP147 MYP19
Myopia 2, Autosomal Dominant MYP127 MYP2
Myopia 20, Autosomal Dominant MYP084 MYP20
Myopia 21, Autosomal Dominant MYP070 MYP21
Myopia 22, Autosomal Dominant MYP075 MYP22
Myopia 23, Autosomal Recessive MYP074 MYP23
Myopia 24, Autosomal Dominant MYP090 MYP24
Myopia 25, Autosomal Dominant MYP117 MYP25
Myopia 26, X-Linked, Female-Limited MYP135 MYP26
Myopia 3, Autosomal Dominant MYP138 MYP3
Myopia 5, Autosomal Dominant MYP141 MYP5
Myopia 6 MYP018 MYP6
Myopia 7 MYP040 MYP7
Myopia 8 MYP041 MYP8
Myopia 9 MYP048 MYP9
Myopia, High, with Cataract and Vitreoretinal Degeneration MYP073 MCVD
Myopic Macular Degeneration MYP060
Myosclerosis, Autosomal Recessive MYS016 MYOSAR
Myosin Storage Myopathy MYS032
Myosinopathies MYS066
Myositis MYS005 IIM
Myositis Fibrosa MYS002
Myositis Ossificans MYS001
Myospherulosis MYS028
Myostatin-Related Muscle Hypertrophy MYS010 MSLHP
Myotonia MYT011
Myotonia Atrophica MYT026
Myotonia Congenita MYT023
Myotonia Congenita, Autosomal Dominant MYT027 MCAD
Myotonia Congenita, Autosomal Recessive MYT029 MCAR
Myotonia with Skeletal Abnormalities and Mental Retardation MYT024
Myotonia, Potassium-Aggravated MYT030 MYOSCN4A
Myotonic Cataract MYT001
Myotonic Disease MYT003
Myotonic Dystrophy MYT002
Myotonic Dystrophy 1 MYT021 DM1
Myotonic Dystrophy 2 MYT020 DM2
Myotonic Myopathy with Cylindrical Spirals MYT028
Myotubular Myopathy with Abnormal Genital Development MYT025
Myringitis Bullosa Hemorrhagica MYR001
Myxedema MYX004
Myxofibrosarcoma MYX013
Myxoid Chondrosarcoma MYX008
Myxoid Leiomyosarcoma MYX006
Myxoid Liposarcoma MYX005 MXLIPO
Myxoid Liposarcoma of the Ovary MYX002
Myxoma, Intracardiac MYX012 INTMYX
Myxomatous Pattern Testicular Yolk Sac Tumor MYX003
Myxopapillary Ependymoma MYX001
Myxosarcoma MYX007
Myxozoa MYX011
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