Disease Name Symbol Acronym
Macdermot-Winter Syndrome MCD004
Machado-Joseph Disease MCH002
Machado-Joseph Disease Type 1 MCH012
Machado-Joseph Disease Type 2 MCH014
Machado-Joseph Disease Type 3 MCH013
Macrocephaly and Epileptic Encephalopathy MCR347
Macrocephaly, Acquired, with Impaired Intellectual Development MCR370
Macrocephaly, Benign Familial MCR031
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation MCR321
Macrocephaly/autism Syndrome MCR096
Macrocephaly/megalencephaly Syndrome, Autosomal Recessive MCR237
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
Macroglobulinemia, Waldenstrom 2 MCR162
Macroglossia MCR037
Macrophage Activation Syndrome MCR225
Macrophagic Myofasciitis MCR039
Macrophthalmia, Colobomatous, with Microcornea MCR317
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
Macrothrombocytopenia Progressive Deafness MCR041
Macrothrombocytopenia with Mitral Valve Insufficiency MCR178
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related MCR125
Macrotrabecular Hepatoblastoma MCR005
Macrozoospermia MCR265
Macs Syndrome MCS006
Macular Amyloidosis MCL047
Macular Degeneration, Age-Related, 1 MCL042
Macular Degeneration, Age-Related, 10 MCL030
Macular Degeneration, Age-Related, 11 MCL032
Macular Degeneration, Age-Related, 12 MCL051
Macular Degeneration, Age-Related, 13 MCL052
Macular Degeneration, Age-Related, 14 MCL078
Macular Degeneration, Age-Related, 15 MCL065
Macular Degeneration, Age-Related, 2 MCL043
Macular Degeneration, Age-Related, 4 MCL038
Macular Degeneration, Age-Related, 5 MCL077
Macular Degeneration, Age-Related, 6 MCL036
Macular Degeneration, Age-Related, 7 MCL041
Macular Degeneration, Age-Related, 8 MCL039
Macular Degeneration, Age-Related, 9 MCL044
Macular Degeneration, Early-Onset MCL058
Macular Degeneration, X-Linked Atrophic MCL029
Macular Dystrophy with Central Cone Involvement MCL057
Macular Dystrophy, Concentric Annular MCL018
Macular Dystrophy, Corneal MCL075
Macular Dystrophy, Dominant Cystoid MCL027
Macular Dystrophy, Fenestrated Sheen Type MCL074
Macular Dystrophy, Patterned, 1 MCL059
Macular Dystrophy, Patterned, 2 MCL071
Macular Dystrophy, Patterned, 3 MCL070
Macular Dystrophy, Retinal, 1, North Carolina Type MCL069
Macular Dystrophy, Retinal, 2 MCL035
Macular Dystrophy, Retinal, 3 MCL026
Macular Dystrophy, Vitelliform, 1 MCL073
Macular Dystrophy, Vitelliform, 2 MCL066
Macular Dystrophy, Vitelliform, 3 MCL060
Macular Dystrophy, Vitelliform, 4 MCL061
Macular Dystrophy, Vitelliform, 5 MCL056
Macular Dystrophy, X-Linked MCL076
Macular Holes MCL003
Macular Keratitis MCL004
Macular Retinal Edema MCL006
Macular Telangiectasia Type 2 MCL079
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
Magic Syndrome MGC006
Magnesium, Elevated Red Cell MGN003
Mahvash Disease MHV001
Main Bronchus Cancer MNB001
Majeed Syndrome MJD001
Major Affective Disorder 1 MJR007
Major Affective Disorder 2 MJR008
Major Affective Disorder 3 MJR021
Major Affective Disorder 4 MJR004
Major Affective Disorder 5 MJR006
Major Affective Disorder 6 MJR003
Major Affective Disorder 7 MJR023
Major Affective Disorder 8 MJR022
Major Affective Disorder 9 MJR024
Major Depressive Disorder MJR001
Major Depressive Disorder 1 MJR013
Major Depressive Disorder 2 MJR014
Mal De Debarquement Syndrome MLD017
Mal De Meleda MLD006
Malakoplakia MLK004
Malaria MLR004
Malaria, Mild MLR020
Male Genital Organ Stricture MLG025
Male Genital Organ Vascular Disease MLG026
Male Infertility MLN007
Male Infertility Due to Acephalic Spermatozoa MLN078
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
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 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
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
Malignant Hyperthermia 1 MLG147
Malignant Hyperthermia 2 MLG148
Malignant Hyperthermia 3 MLG149
Malignant Hyperthermia 4 MLG150
Malignant Hyperthermia 5 MLG151
Malignant Hyperthermia 6 MLG152
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
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 Surface Epithelial-Stromal Neoplasm MLG076
Malignant Parietal Pleura Tumor MLG030
Malignant Pediatric Adrenal Gland Pheochromocytoma MLG159
Malignant Peripheral Nerve Sheath Tumor MLG077
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
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
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
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
Mammastatin MMM005
Mammographic Density MMM006
Man1b1-Cdg MN1002
Mandibular Arteriovenous Malformation MND008
Mandibular Cancer MND001
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome MND021
Mandibuloacral Dysplasia with Type a Lipodystrophy MND003
Mandibuloacral Dysplasia with Type B Lipodystrophy MND002
Mandibulofacial Dysostosis Syndrome, Bauru Type MND029
Mandibulofacial Dysostosis with Alopecia MND025
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia MND027
Mandibulofacial Dysostosis with Mental Retardation MND028
Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant MND030
Mandibulofacial Dysostosis, Guion-Almeida Type MND020
Manganese Poisoning MNG007
Manitoba Oculotrichoanal Syndrome MNT006
Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type MNN046
Mannose-Binding Lectin Deficiency MNN034
Mannose-Binding Lectin Protein Deficiency MNN041
Mannosidosis MNN018
Mannosidosis, Alpha B, Lysosomal MNN047
Mannosidosis, Beta a, Lysosomal MNN019
Manouvrier Syndrome MNV001
Mansonelliasis MNS001
Mantle Cell Lymphoma MNT001
Maple Bark Strippers' Lung MPL002
Maple Syrup Urine Disease MPL001
Maple Syrup Urine Disease, Mild Variant MPL011
Marantic Endocarditis MRN001
Marasmus MRS001
Marburg Acute Multiple Sclerosis MRB005
Marburg Hemorrhagic Fever MRB001
Marchiafava Bignami Disease MRC001
Marcus Gunn Phenomenon MRC002
Marden Walker Like Syndrome MRD001
Marden-Walker Syndrome MRD002
Marek Disease MRK002
Marfan Syndrome MRF001
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
Marfanoid-Progeroid-Lipodystrophy Syndrome MRF021
Marginal Corneal Ulcer MRG002
Marginal Glioneuronal Heterotopia MRG004
Marginal Zone B-Cell Lymphoma MRG003
Marie Unna Congenital Hypotrichosis MRN005
Marin-Amat Syndrome MRN008
Marinesco-Sjogren Syndrome MRN003
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
Marshall Syndrome MRS002
Marshall-Smith Syndrome MRS004
Marsili Syndrome MRS009
Martinez Monasterio Pinheiro Syndrome MRT006
Martinez-Frias Syndrome MRT009
Martsolf Syndrome MRT007
Masa Syndrome MSS001
Masp2 Deficiency MSP001
Mass Syndrome MSS002
Massa Casaer Ceulemans Syndrome MSS003
Mast Cell Activation Syndrome MST020
Mast Cell Neoplasm MST004
Mast Syndrome MST006
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
Mastoiditis MST019
Maternal Hyperphenylalaninemia MTR016
Maternal Hyperthermia-Induced Birth Defects MTR084
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
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
Maturity-Onset Diabetes of the Young, Type 1 MTR018
Maturity-Onset Diabetes of the Young, Type 10 MTR044
Maturity-Onset Diabetes of the Young, Type 11 MTR039
Maturity-Onset Diabetes of the Young, Type 13 MTR075
Maturity-Onset Diabetes of the Young, Type 14 MTR074
Maturity-Onset Diabetes of the Young, Type 2 MTR019
Maturity-Onset Diabetes of the Young, Type 3 MTR020
Maturity-Onset Diabetes of the Young, Type 4 MTR021
Maturity-Onset Diabetes of the Young, Type 6 MTR023
Maturity-Onset Diabetes of the Young, Type 7 MTR024
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction MTR082
Maturity-Onset Diabetes of the Young, Type 9 MTR026
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 Neoplasm MXL009
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
May-Thurner Syndrome MYT019
Mazabraud Syndrome MZB001
Mbd25-Related Intellectual Disability MBD002
Mbd5 Haploinsufficiency MBD001
Mccune-Albright Syndrome MCC012
Mcdonough Syndrome MCD002
Mcdowall Syndrome MCD003
Mcgillivray Syndrome MCG001
Mckusick-Kaufman Syndrome MCK005
Mcleod Syndrome MCL009
Mcpherson Clemens Syndrome MCP018
Mcpherson Robertson Cammarano Syndrome MCP019
Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency MCT002
Mda5 Deficiency MD5001
Meacham Syndrome MCH011
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
Meckel Syndrome 13 MCK028
Meckel Syndrome, Type 1 MCK013
Meckel Syndrome, Type 10 MCK035
Meckel Syndrome, Type 11 MCK020
Meckel Syndrome, Type 2 MCK031
Meckel Syndrome, Type 3 MCK032
Meckel Syndrome, Type 4 MCK033
Meckel Syndrome, Type 5 MCK014
Meckel Syndrome, Type 6 MCK012
Meckel Syndrome, Type 7 MCK030
Meckel Syndrome, Type 8 MCK034
Meckel Syndrome, Type 9 MCK036
Meckel's Diverticulitis MCK004
Meckel's Diverticulum Cancer MCK001
Meconium Aspiration Syndrome MCN007
Meconium Ileus MCN017
Mecp2-Related Severe Neonatal Encephalopathy MCP022
Mecr-Related Neurologic Disorder MCR373
Med12-Related Disorders MD1001
Med13l Haploinsufficiency Syndrome MD1003
Med23 MD2001
Medeira-Dennis-Donnai Syndrome MDR001
Medial Medullary Syndrome MDL007
Median Arcuate Ligament Syndrome MDN008
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
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
Medrano Roldan Syndrome MDR002
Medullary Colon Carcinoma MDL026
Medullary Cystic Kidney Disease 1 MDL008
Medullary Cystic Kidney Disease 2 MDL021
Medullary Sponge Kidney MDL009
Medulloadrenal Hyperfunction MDL001
Medulloblastoma MDL005
Medulloepithelioma MDL002
Medullomyoblastoma MDL003
Meester-Loeys Syndrome MST021
Megacolon MGC001
Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations MGC007
Megacystis-Megaureter Syndrome MGC005
Megaepiphyseal Dwarfism MGP001
Megaesophagus MGS001
Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) MGK005
Megakaryocytic Leukemia MGK001
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 MGL009
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a MGL010
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b, Remitting, with or Without Mental Retardation MGL011
Megalencephaly MGL013
Megalencephaly with Dysmyelination MGL037
Megalencephaly, Autosomal Dominant MGL035
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome MGL038
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 MGL030
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 MGL028
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 MGL029
Megaloblastic Anemia MGL001
Megaloblastic Anemia 1 MGL018
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency MGL012
Megalocornea MGL003
Megalocornea - Spherophakia - Secondary Glaucoma MGL005
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
Mehta Lewis Patton Syndrome MHT001
Meibomian Cyst MBM001
Meier-Gorlin Syndrome 1 MRG008
Meier-Gorlin Syndrome 2 MRG009
Meier-Gorlin Syndrome 3 MRG010
Meier-Gorlin Syndrome 4 MRG011
Meier-Gorlin Syndrome 5 MRG012
Meier-Gorlin Syndrome 6 MRG014
Meier-Gorlin Syndrome 7 MRG015
Meier-Gorlin Syndrome 8 MRG016
Melancholia MLN003
Melanoacanthoma MLN005
Melanocytic Lesions of Cns MLN015
Melanocytic Nevus Syndrome, Congenital MLN065
Melanocytic Psammomatous Mpnst MLN006
Melanoma MLN008
Melanoma in Congenital Melanocytic Nevus MLN079
Melanoma Metastasis MLN013
Melanoma of Soft Tissue MLN064
Melanoma Tumor Antigen Gp90 MLN071
Melanoma, Cutaneous Malignant 1 MLN066
Melanoma, Cutaneous Malignant 10 MLN055
Melanoma, Cutaneous Malignant 2 MLN067
Melanoma, Cutaneous Malignant 3 MLN075
Melanoma, Cutaneous Malignant 4 MLN074
Melanoma, Cutaneous Malignant 5 MLN076
Melanoma, Cutaneous Malignant 6 MLN042
Melanoma, Cutaneous Malignant 7 MLN040
Melanoma, Cutaneous Malignant 8 MLN043
Melanoma, Cutaneous Malignant 9 MLN077
Melanoma, Malignant Familial Intraocular MLN068
Melanoma, Uveal MLN069
Melanoma, Uveal 1 MLN039
Melanoma, Uveal 2 MLN041
Melanoma-Associated Retinopathy MLN046
Melanoma-Astrocytoma Syndrome MLN070
Melanoma-Pancreatic Cancer Syndrome MLN047
Melanomatosis MLN002
Melanosis, Neurocutaneous MLN073
Melanotic Medulloblastoma MLN004
Melanotic Neurilemmoma MLN009
Melanotic Neuroectodermal Tumor MLN001
Melhem Fahl Syndrome MLH001
Melioidosis MLD001
Melkersson-Rosenthal Syndrome MLK003
Melnick-Needles Syndrome MLN014
Melon Allergy MLN063
Melorheostosis MLR003
Melorheostosis with Osteopoikilosis MLR010
Melorheostosis, Isolated MLR023
Melphalan Allergy MLP008
Membranoproliferative Glomerulonephritis MMB001
Membranoproliferative Glomerulonephritis, X-Linked MMB013
Membranous Cranial Ossification, Delayed MMB012
Membranous Nephropathy MMB011
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
Meniere Disease MNR012
Meningeal Melanocytoma MNN001
Meningeal Melanoma MNN010
Meningeal Melanomatosis MNN008
Meninges Hemangiopericytoma MNN006
Meninges Sarcoma MNN011
Meningioma, Familial MNN043
Meningioma, Radiation-Induced MNN042
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
Menke-Hennekam Syndrome 1 MNK005
Menke-Hennekam Syndrome 2 MNK006
Menkes Disease MNK001
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
Mental Health Wellness 2 MNT313
Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects MNT266
Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia MNT046
Mental Retardation and Psoriasis MNT255
Mental Retardation Smith Fineman Myers Type MNT028
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
Mental Retardation with Optic Atrophy, Deafness, and Seizures MNT308
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
Mental Retardation, Autosomal Dominant 10 MNT186
Mental Retardation, Autosomal Dominant 11 MNT184
Mental Retardation, Autosomal Dominant 13 MNT143
Mental Retardation, Autosomal Dominant 18 MNT157
Mental Retardation, Autosomal Dominant 20 MNT319
Mental Retardation, Autosomal Dominant 21 MNT179
Mental Retardation, Autosomal Dominant 22 MNT158
Mental Retardation, Autosomal Dominant 23 MNT211
Mental Retardation, Autosomal Dominant 24 MNT214
Mental Retardation, Autosomal Dominant 26 MNT212
Mental Retardation, Autosomal Dominant 27 MNT322
Mental Retardation, Autosomal Dominant 29 MNT222
Mental Retardation, Autosomal Dominant 30 MNT219
Mental Retardation, Autosomal Dominant 31 MNT226
Mental Retardation, Autosomal Dominant 32 MNT241
Mental Retardation, Autosomal Dominant 33 MNT240
Mental Retardation, Autosomal Dominant 34 MNT238
Mental Retardation, Autosomal Dominant 35 MNT239
Mental Retardation, Autosomal Dominant 36 MNT245
Mental Retardation, Autosomal Dominant 38 MNT246
Mental Retardation, Autosomal Dominant 39 MNT236
Mental Retardation, Autosomal Dominant 40 MNT242
Mental Retardation, Autosomal Dominant 41 MNT272
Mental Retardation, Autosomal Dominant 42 MNT262
Mental Retardation, Autosomal Dominant 43 MNT280
Mental Retardation, Autosomal Dominant 44 MNT273
Mental Retardation, Autosomal Dominant 45 MNT286
Mental Retardation, Autosomal Dominant 46 MNT278
Mental Retardation, Autosomal Dominant 47 MNT279
Mental Retardation, Autosomal Dominant 48 MNT323
Mental Retardation, Autosomal Dominant 49 MNT324
Mental Retardation, Autosomal Dominant 50 MNT326
Mental Retardation, Autosomal Dominant 51 MNT327
Mental Retardation, Autosomal Dominant 52 MNT328
Mental Retardation, Autosomal Dominant 53 MNT329
Mental Retardation, Autosomal Dominant 54 MNT330
Mental Retardation, Autosomal Dominant 55, with Seizures MNT331
Mental Retardation, Autosomal Dominant 56 MNT332
Mental Retardation, Autosomal Dominant 57 MNT334
Mental Retardation, Autosomal Dominant 58 MNT337
Mental Retardation, Autosomal Dominant 6, with or Without Seizures MNT320
Mental Retardation, Autosomal Dominant 7 MNT185
Mental Retardation, Autosomal Recessive 14 MNT154
Mental Retardation, Autosomal Recessive 15 MNT150
Mental Retardation, Autosomal Recessive 16 MNT167
Mental Retardation, Autosomal Recessive 18 MNT151
Mental Retardation, Autosomal Recessive 19 MNT182
Mental Retardation, Autosomal Recessive 2 MNT155
Mental Retardation, Autosomal Recessive 23 MNT170
Mental Retardation, Autosomal Recessive 24 MNT162
Mental Retardation, Autosomal Recessive 25 MNT172
Mental Retardation, Autosomal Recessive 27 MNT177
Mental Retardation, Autosomal Recessive 28 MNT165
Mental Retardation, Autosomal Recessive 29 MNT161
Mental Retardation, Autosomal Recessive 30 MNT163
Mental Retardation, Autosomal Recessive 31 MNT160
Mental Retardation, Autosomal Recessive 33 MNT180
Mental Retardation, Autosomal Recessive 34, with Variant Lissencephaly MNT283
Mental Retardation, Autosomal Recessive 35 MNT181
Mental Retardation, Autosomal Recessive 36 MNT183
Mental Retardation, Autosomal Recessive 37 MNT321
Mental Retardation, Autosomal Recessive 38 MNT176
Mental Retardation, Autosomal Recessive 39 MNT166
Mental Retardation, Autosomal Recessive 40 MNT213
Mental Retardation, Autosomal Recessive 41 MNT216
Mental Retardation, Autosomal Recessive 42 MNT210
Mental Retardation, Autosomal Recessive 43 MNT215
Mental Retardation, Autosomal Recessive 44 MNT221
Mental Retardation, Autosomal Recessive 45 MNT220
Mental Retardation, Autosomal Recessive 46 MNT227
Mental Retardation, Autosomal Recessive 47 MNT225
Mental Retardation, Autosomal Recessive 48 MNT234
Mental Retardation, Autosomal Recessive 49 MNT244
Mental Retardation, Autosomal Recessive 5 MNT145
Mental Retardation, Autosomal Recessive 50 MNT243
Mental Retardation, Autosomal Recessive 51 MNT263
Mental Retardation, Autosomal Recessive 52 MNT264
Mental Retardation, Autosomal Recessive 53 MNT270
Mental Retardation, Autosomal Recessive 54 MNT277
Mental Retardation, Autosomal Recessive 55 MNT282
Mental Retardation, Autosomal Recessive 56 MNT284
Mental Retardation, Autosomal Recessive 57 MNT287
Mental Retardation, Autosomal Recessive 58 MNT285
Mental Retardation, Autosomal Recessive 59 MNT281
Mental Retardation, Autosomal Recessive 60 MNT275
Mental Retardation, Autosomal Recessive 61 MNT325
Mental Retardation, Autosomal Recessive 63 MNT335
Mental Retardation, Autosomal Recessive 64 MNT336
Mental Retardation, Autosomal Recessive 65 MNT338
Mental Retardation, Autosomal Recessive 66 MNT339
Mental Retardation, Buenos Aires Type MNT256
Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma MNT317
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
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy MNT252
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome MNT318
Mental Retardation, X-Linked 100 MNT223
Mental Retardation, X-Linked 101 MNT224
Mental Retardation, X-Linked 102 MNT248
Mental Retardation, X-Linked 103 MNT289
Mental Retardation, X-Linked 104 MNT267
Mental Retardation, X-Linked 105 MNT274
Mental Retardation, X-Linked 106 MNT294
Mental Retardation, X-Linked 107 MNT333
Mental Retardation, X-Linked 12 MNT305
Mental Retardation, X-Linked 21 MNT301
Mental Retardation, X-Linked 23 MNT204
Mental Retardation, X-Linked 42 MNT205
Mental Retardation, X-Linked 50 MNT194
Mental Retardation, X-Linked 53 MNT202
Mental Retardation, X-Linked 73 MNT247
Mental Retardation, X-Linked 92 MNT196
Mental Retardation, X-Linked 96 MNT195
Mental Retardation, X-Linked 97 MNT200
Mental Retardation, X-Linked 98 MNT198
Mental Retardation, X-Linked 99 MNT218
Mental Retardation, X-Linked 99, Syndromic, Female-Restricted MNT290
Mental Retardation, X-Linked, Associated with Fragile Site Fraxe MNT307
Mental Retardation, X-Linked, Syndromic 13 MNT135
Mental Retardation, X-Linked, Syndromic 17 MNT191
Mental Retardation, X-Linked, Syndromic 32 MNT207
Mental Retardation, X-Linked, Syndromic 33 MNT295
Mental Retardation, X-Linked, Syndromic 34 MNT296
Mental Retardation, X-Linked, Syndromic 9 MNT197
Mental Retardation, X-Linked, Syndromic, 35 MNT298
Mental Retardation, X-Linked, Syndromic, Bain Type MNT269
Mental Retardation, X-Linked, Syndromic, Cabezas Type MNT303
Mental Retardation, X-Linked, Syndromic, Christianson Type MNT302
Mental Retardation, X-Linked, Syndromic, Chudley-Schwartz Type MNT201
Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type MNT228
Mental Retardation, X-Linked, Syndromic, Hedera Type MNT192
Mental Retardation, X-Linked, Syndromic, Houge Type MNT306
Mental Retardation, X-Linked, Syndromic, Martin-Probst Type MNT146
Mental Retardation, X-Linked, Syndromic, Nascimento Type MNT056
Mental Retardation, X-Linked, Syndromic, Raymond Type MNT057
Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type MNT310
Mental Retardation, X-Linked, Syndromic, Turner Type MNT058
Mental Retardation, X-Linked, Syndromic, Wu Type MNT258
Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance MNT229
Mental Retardation, X-Linked, with Craniofacial Dysmorphism MNT257
Mental Retardation, X-Linked, with or Without Seizures, Arx-Related MNT304
Mental Retardation, X-Linked, with Panhypopituitarism MNT300
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 MNT309
Mepivacaine Allergy MPV003
Meralgia Paraesthetica, Familial MRL006
Meralgia Paresthetica MRL001
Mercaptolactate-Cysteine Disulfiduria MRC009
Mercury Poisoning MRC003
Merkel Cell Carcinoma MRK001
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
Mesomelic Dysplasia, Savarirayan Type MSM019
Mesomelic Limb Shortening and Bowing MSM018
Mesothelioma, Malignant MST023
Metabolic Acidosis MTB004
Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration MTB008
Metabolic Crises, Recurrent, with Variable Encephalomyopathic Features and Neurologic Regression MTB009
Metacarpal 4-5 Fusion MTC100
Metachondromatosis MTC018
Metachromasia of Fibroblasts MTC131
Metachromatic Leukodystrophy MTC003
Metachromatic Leukodystrophy Due to Saposin B Deficiency MTC019
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
Metaphyseal Anadysplasia 2 MTP014
Metaphyseal Chondrodysplasia with Cone-Shaped Epiphyses, Normal Hair, and Normal Hands MTP007
Metaphyseal Chondrodysplasia, Jansen Type MTP034
Metaphyseal Chondrodysplasia, Kaitila Type MTP017
Metaphyseal Chondrodysplasia, Others MTP008
Metaphyseal Chondrodysplasia, Pena Type MTP035
Metaphyseal Chondrodysplasia, Schmid Type MTP025
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
Metaphyseal Dysplasia Without Hypotrichosis MTP003
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy MTP036
Metaphyseal Dysplasia, Braun-Tinschert Type MTP021
Metaphyseal Dysplasia, Spahr Type MTP028
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
Metatypical Basal Cell Carcinoma MTT001
Methane Production MTH071
Methanol Poisoning MTH047
Methemoglobin Reductase Deficiency MTH072
Methemoglobinemia MTH007
Methemoglobinemia and Ambiguous Genitalia MTH082
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase MTH026
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
Methionine Malabsorption Syndrome MTH075
Methotrexate Toxicity or Dose Selection MTH061
Methotrexate-Associated Lymphoproliferation MTH001
Methotrexate-Associated Lymphoproliferative Disorders MTH049
Methyl Isocyanate Allergic Asthma MTH085
Methylmalonate Semialdehyde Dehydrogenase Deficiency MTH013
Methylmalonic Acidemia MTH008
Methylmalonic Acidemia and Homocysteinemia, Cblx Type MTH079
Methylmalonic Acidemia Due to Transcobalamin Receptor Defect MTH069
Methylmalonic Acidemia with Homocystinuria MTH021
Methylmalonic Acidemia with Homocystinuria Type Cblj MTH067
Methylmalonic Aciduria and Homocystinuria Type Cble MTH003
Methylmalonic Aciduria and Homocystinuria Type Cblg MTH002
Methylmalonic Aciduria and Homocystinuria, Cblc Type MTH054
Methylmalonic Aciduria and Homocystinuria, Cbld Type MTH055
Methylmalonic Aciduria and Homocystinuria, Cblf Type MTH056
Methylmalonic Aciduria and Homocystinuria, Cblj Type MTH051
Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency MTH076
Methylmalonic Aciduria, Cbla Type MTH077
Methylmalonic Aciduria, Cblb Type MTH078
Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect MTH068
Methylmalonyl-Coa Epimerase Deficiency MTH040
Methylmalonyl-Coenzyme a Mutase Deficiency MTH025
Metopic Ridging-Ptosis-Facial Dysmorphism Syndrome MTP038
Mevalonic Aciduria MVL001
Michels Caskey Syndrome MCH009
Microbrachycephaly Ptosis Cleft Lip MCR042
Microcephalic Osteodysplastic Primordial Dwarfism, Type I MCR240
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii MCR258
Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii MCR331
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
Microcephaly 10, Primary, Autosomal Recessive MCR223
Microcephaly 11, Primary, Autosomal Recessive MCR249
Microcephaly 12, Primary, Autosomal Recessive MCR246
Microcephaly 13, Primary, Autosomal Recessive MCR236
Microcephaly 14, Primary, Autosomal Recessive MCR270
Microcephaly 15, Primary, Autosomal Recessive MCR269
Microcephaly 16, Primary, Autosomal Recessive MCR314
Microcephaly 17, Primary, Autosomal Recessive MCR320
Microcephaly 18, Primary, Autosomal Dominant MCR322
Microcephaly 19, Primary, Autosomal Recessive MCR356
Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations MCR222
Microcephaly 20, Primary, Autosomal Recessive MCR360
Microcephaly 21, Primary, Autosomal Recessive MCR361
Microcephaly 22, Primary, Autosomal Recessive MCR362
Microcephaly 23, Primary, Autosomal Recessive MCR363
Microcephaly 24, Primary, Autosomal Recessive MCR368
Microcephaly 25, Primary, Autosomal Recessive MCR372
Microcephaly 3, Primary, Autosomal Recessive MCR248
Microcephaly 4, Primary, Autosomal Recessive MCR254
Microcephaly 5, Primary, Autosomal Recessive MCR239
Microcephaly 6, Primary, Autosomal Recessive MCR250
Microcephaly 7, Primary, Autosomal Recessive MCR238
Microcephaly 8, Primary, Autosomal Recessive MCR243
Microcephaly 9, Primary, Autosomal Recessive MCR255
Microcephaly and Chorioretinopathy 1 MCR282
Microcephaly and Chorioretinopathy 2 MCR283
Microcephaly and Chorioretinopathy 3 MCR284
Microcephaly and Chorioretinopathy, Autosomal Recessive, 1 MCR259
Microcephaly and Chorioretinopathy, Autosomal Recessive, 2 MCR244
Microcephaly and Chorioretinopathy, Autosomal Recessive, 3 MCR272
Microcephaly Brain Defect Spasticity Hypernatremia MCR046
Microcephaly Chorioretinopathy Recessive Form MCR048
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
Microcephaly with Simplified Gyral Pattern MCR345
Microcephaly with Spastic Quadriplegia MCR060
Microcephaly, Amish Type MCR257
Microcephaly, Autosomal Dominant MCR329
Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum MCR369
Microcephaly, Cerebellar Hypoplasia, and Cardiac Conduction Defect Syndrome MCR311
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis MCR315
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
Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation MCR344
Microcephaly, Facial Dysmorphism, Renal Agenesis, and Ambiguous Genitalia Syndrome MCR366
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations MCR371
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
Microcephaly, Progressive, with Seizures and Cerebral and Cerebellar Atrophy MCR355
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract MCR341
Microcephaly, Seizures, and Developmental Delay MCR064
Microcephaly, Seizures, Spasticity, and Brain Calcifications MCR333
Microcephaly, Severe, with Skeletal Anomalies Including Posterior Rib-Gap Defects MCR343
Microcephaly, Short Stature, and Impaired Glucose Metabolism 1 MCR323
Microcephaly, Short Stature, and Impaired Glucose Metabolism 2 MCR316
Microcephaly, Short Stature, and Limb Abnormalities MCR327
Microcephaly, Short Stature, and Polymicrogyria with or Without Seizures MCR354
Microcephaly-Capillary Malformation Syndrome MCR183
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
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
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
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
Microencephaly MCR374
Microform Holoprosencephaly MCR173
Microgastria Limb Reduction Defect MCR073
Microgastria-Limb Reduction Defects Association MCR310
Microglandular Adenosis MCR019
Microglandular Adenosis of Breast MCR012
Microhydranencephaly MCR025
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
Microphthalmia, Isolated 1 MCR124
Microphthalmia, Isolated 2 MCR137
Microphthalmia, Isolated 3 MCR114
Microphthalmia, Isolated 4 MCR109
Microphthalmia, Isolated 5 MCR122
Microphthalmia, Isolated 6 MCR211
Microphthalmia, Isolated 7 MCR108
Microphthalmia, Isolated 8 MCR219
Microphthalmia, Isolated, with Cataract 1 MCR330
Microphthalmia, Isolated, with Coloboma 1 MCR338
Microphthalmia, Isolated, with Coloboma 10 MCR271
Microphthalmia, Isolated, with Coloboma 2 MCR346
Microphthalmia, Isolated, with Coloboma 3 MCR349
Microphthalmia, Isolated, with Coloboma 4 MCR335
Microphthalmia, Isolated, with Coloboma 5 MCR350
Microphthalmia, Isolated, with Coloboma 6 MCR352
Microphthalmia, Isolated, with Coloboma 7 MCR210
Microphthalmia, Isolated, with Coloboma 9 MCR214
Microphthalmia, Isolated, with Corectopia MCR087
Microphthalmia, Syndromic 1 MCR263
Microphthalmia, Syndromic 10 MCR312
Microphthalmia, Syndromic 11 MCR217
Microphthalmia, Syndromic 12 MCR212
Microphthalmia, Syndromic 13 MCR228
Microphthalmia, Syndromic 2 MCR261
Microphthalmia, Syndromic 3 MCR241
Microphthalmia, Syndromic 4 MCR262
Microphthalmia, Syndromic 5 MCR252
Microphthalmia, Syndromic 6 MCR251
Microphthalmia, Syndromic 8 MCR245
Microphthalmia, Syndromic 9 MCR256
Microphthalmia/anophthalmia/coloboma Spectrum MCR273
Microphthalmia/coloboma and Skeletal Dysplasia Syndrome MCR324
Microscopic Breast Papilloma MCR009
Microscopic Colitis MCR191
Microscopic Polyangiitis MCR088
Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or Without Secondary Glaucoma MCR253
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
Microtia-Anotia MCR093
Microtriplication 11q24.1 MCR186
Microvascular Complications of Diabetes 1 MCR129
Microvascular Complications of Diabetes 2 MCR112
Microvascular Complications of Diabetes 3 MCR113
Microvascular Complications of Diabetes 4 MCR133
Microvascular Complications of Diabetes 5 MCR115
Microvascular Complications of Diabetes 6 MCR130
Microvascular Complications of Diabetes 7 MCR120
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
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
Midline Malformations, Multiple, with Limb Abnormalities and Hypopituitarism MDL027
Midphalangeal Hair MDP001
Migraine with Aura MGR003
Migraine with Aura 7 MGR025
Migraine with Aura 9 MGR027
Migraine with Brainstem Aura MGR035
Migraine with or Without Aura 1 MGR028
Migraine with or Without Aura 10 MGR038
Migraine with or Without Aura 11 MGR039
Migraine with or Without Aura 12 MGR040
Migraine with or Without Aura 13 MGR042
Migraine with or Without Aura 2 MGR036
Migraine with or Without Aura 3 MGR022
Migraine with or Without Aura 5 MGR024
Migraine with or Without Aura 6 MGR033
Migraine with or Without Aura 8 MGR037
Migraine Without Aura MGR001
Migraine Without Aura 4 MGR023
Migraine, Familial Hemiplegic, 1 MGR032
Migraine, Familial Hemiplegic, 2 MGR030
Migraine, Familial Hemiplegic, 3 MGR031
Mikati-Najjar-Sahli Syndrome MKT001
Mikulicz Disease MKL001
Mild Hyperphenylalaninemia MLD011
Mild Phenylketonuria MLD010
Mild Pre-Eclampsia MLD002
Miles-Carpenter Syndrome MLS013
Milia, Multiple Eruptive MLM001
Miliaria MLR009
Miliaria Crystallina MLR026
Miliaria Profunda MLR025
Miliaria Pustulosa MLR024
Miliaria Rubra MLR001
Miliary Tuberculosis MLR002
Milk Allergy MLK006
Milker's Nodule MLK001
Miller Fisher Syndrome MLL002
Miller-Dieker Lissencephaly Syndrome MLL018
Mills Syndrome MLL015
Milner Khallouf Gibson Syndrome MLN017
Mineral Metabolism Disease MNR003
Mini Stroke MNS002
Minicore Myopathy with External Ophthalmoplegia MNC011
Minicore Myopathy, Antenatal Onset, with Arthrogryposis MNC012
Minimal Pigment Oculocutaneous Albinism Type 1 MNM005
Minor Vestibular Glands Adenoma MNR001
Mirage Syndrome MRG013
Mirizzi Syndrome MRZ001
Mirror Agnosia MRR002
Mirror Movements 1 MRR011
Mirror Movements 2 MRR010
Mirror Movements 3 MRR012
Mirror Movements 4 MRR015
Mirror Polydactyly Segmentation and Limbs Defects MRR005
Mirror Polydactyly-Vertebral Segmentation-Limbs Defects Syndrome MRR013
Mismatch Repair Cancer Syndrome MSM014
Misophonia MSP003
Mitchell-Riley Syndrome MTC096
Mite Infestation MTN002
Mitochondrial Complex I Deficiency, Mitochondrial Type 1 MTC149
Mitochondrial Complex I Deficiency, Nuclear Type 1 MTC146
Mitochondrial Complex I Deficiency, Nuclear Type 10 MTC158
Mitochondrial Complex I Deficiency, Nuclear Type 11 MTC159
Mitochondrial Complex I Deficiency, Nuclear Type 12 MTC147
Mitochondrial Complex I Deficiency, Nuclear Type 13 MTC160
Mitochondrial Complex I Deficiency, Nuclear Type 14 MTC161
Mitochondrial Complex I Deficiency, Nuclear Type 15 MTC162
Mitochondrial Complex I Deficiency, Nuclear Type 16 MTC163
Mitochondrial Complex I Deficiency, Nuclear Type 17 MTC164
Mitochondrial Complex I Deficiency, Nuclear Type 18 MTC165
Mitochondrial Complex I Deficiency, Nuclear Type 19 MTC166
Mitochondrial Complex I Deficiency, Nuclear Type 2 MTC152
Mitochondrial Complex I Deficiency, Nuclear Type 20 MTC151
Mitochondrial Complex I Deficiency, Nuclear Type 21 MTC167
Mitochondrial Complex I Deficiency, Nuclear Type 22 MTC168
Mitochondrial Complex I Deficiency, Nuclear Type 23 MTC169
Mitochondrial Complex I Deficiency, Nuclear Type 24 MTC170
Mitochondrial Complex I Deficiency, Nuclear Type 25 MTC171
Mitochondrial Complex I Deficiency, Nuclear Type 26 MTC172
Mitochondrial Complex I Deficiency, Nuclear Type 27 MTC173
Mitochondrial Complex I Deficiency, Nuclear Type 28 MTC174
Mitochondrial Complex I Deficiency, Nuclear Type 29 MTC175
Mitochondrial Complex I Deficiency, Nuclear Type 30 MTC148
Mitochondrial Complex I Deficiency, Nuclear Type 31 MTC176
Mitochondrial Complex I Deficiency, Nuclear Type 32 MTC177
Mitochondrial Complex I Deficiency, Nuclear Type 33 MTC178
Mitochondrial Complex I Deficiency, Nuclear Type 4 MTC153
Mitochondrial Complex I Deficiency, Nuclear Type 6 MTC154
Mitochondrial Complex I Deficiency, Nuclear Type 7 MTC155
Mitochondrial Complex I Deficiency, Nuclear Type 8 MTC156
Mitochondrial Complex I Deficiency, Nuclear Type 9 MTC157
Mitochondrial Complex Ii Deficiency MTC020
Mitochondrial Complex Iii Deficiency MTC008
Mitochondrial Complex Iii Deficiency, Nuclear Type 1 MTC085
Mitochondrial Complex Iii Deficiency, Nuclear Type 2 MTC091
Mitochondrial Complex Iii Deficiency, Nuclear Type 3 MTC089
Mitochondrial Complex Iii Deficiency, Nuclear Type 4 MTC087
Mitochondrial Complex Iii Deficiency, Nuclear Type 6 MTC090
Mitochondrial Complex Iii Deficiency, Nuclear Type 7 MTC095
Mitochondrial Complex Iii Deficiency, Nuclear Type 8 MTC094
Mitochondrial Complex Iii Deficiency, Nuclear Type 9 MTC098
Mitochondrial Complex Iv Deficiency MTC097
Mitochondrial Complex V Deficiency, Mitochondrial Type 1 MTC150
Mitochondrial Complex V Deficiency, Nuclear Type 1 MTC029
Mitochondrial Complex V Deficiency, Nuclear Type 2 MTC068
Mitochondrial Complex V Deficiency, Nuclear Type 3 MTC030
Mitochondrial Complex V Deficiency, Nuclear Type 4 MTC137
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
Mitochondrial Dna Depletion Syndrome 11 MTC078
Mitochondrial Dna Depletion Syndrome 12a MTC142
Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant MTC139
Mitochondrial Dna Depletion Syndrome 12b MTC143
Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive MTC138
Mitochondrial Dna Depletion Syndrome 13 MTC088
Mitochondrial Dna Depletion Syndrome 14 MTC126
Mitochondrial Dna Depletion Syndrome 15 MTC129
Mitochondrial Dna Depletion Syndrome 2 MTC062
Mitochondrial Dna Depletion Syndrome 3 MTC063
Mitochondrial Dna Depletion Syndrome 4a MTC056
Mitochondrial Dna Depletion Syndrome 4b MTC055
Mitochondrial Dna Depletion Syndrome 5 MTC059
Mitochondrial Dna Depletion Syndrome 6 MTC058
Mitochondrial Dna Depletion Syndrome 7 MTC054
Mitochondrial Dna Depletion Syndrome 8a MTC065
Mitochondrial Dna Depletion Syndrome 9 MTC060
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
Mitochondrial Dna-Associated Leigh Syndrome and Narp MTC015
Mitochondrial Dna-Related Cardiomyopathy and Hearing Loss MTC179
Mitochondrial Dna-Related Dystonia MTC180
Mitochondrial Dna-Related Progressive External Ophthalmoplegia MTC181
Mitochondrial Encephalomyopathy MTC004
Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes MTC023
Mitochondrial Genetic Disorders MTC024
Mitochondrial Import-Stimulating Factor MTC135
Mitochondrial Intermembrane Space Protein Tim12, Yeast, Homolog of MTC136
Mitochondrial Membrane Protein-Associated Neurodegeneration MTC036
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
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes MTC114
Mitochondrial Myopathy, Episodic, with or Without Optic Atrophy and Reversible Leukoencephalopathy MTC145
Mitochondrial Myopathy, Infantile, Transient MTC116
Mitochondrial Myopathy, Lethal, Infantile MTC115
Mitochondrial Neurogastrointestinal Encephalomyopathy MTC111
Mitochondrial Non-Syndromic Sensorineural Deafness MTC106
Mitochondrial Phosphate Carrier Deficiency MTC037
Mitochondrial Pyruvate Carrier Deficiency MTC079
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency MTC108
Mitochondrial Trifunctional Protein Deficiency MTC027
Mitral Atresia MTR027
Mitral Valve Agenesis MTR068
Mitral Valve Disease MTR012
Mitral Valve Insufficiency MTR002
Mitral Valve Prolapse 1 MTR080
Mitral Valve Prolapse 2 MTR077
Mitral Valve Prolapse 3 MTR083
Mitral Valve Prolapse, Familial, Autosomal Dominant MTR029
Mitral Valve Prolapse, Familial, X-Linked MTR030
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
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
Miyoshi Muscular Dystrophy 2 MYS019
Miyoshi Muscular Dystrophy 3 MYS014
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
Moebius Syndrome-Axonal Neuropathy-Hypogonadotropic Hypogonadism Syndrome MBS006
Mohr Syndrome MHR002
Mohr-Tranebjaerg Syndrome MHR001
Mollaret Meningitis MLL006
Molluscum Contagiosum MLL001
Moloney Syndrome MLN018
Molybdenum Cofactor Deficiency MLY001
Molybdenum Cofactor Deficiency, Complementation Group a MLY008
Molybdenum Cofactor Deficiency, Complementation Group B MLY009
Molybdenum Cofactor Deficiency, Complementation Group C MLY010
Momo Syndrome MMS001
Monckeberg Arteriosclerosis MNC003
Mondini Dysplasia MND005
Mondor Disease MND006
Mongolian Spot MNG001
Monieziasis MNZ001
Monilethrix MNL001
Monkeypox MNK002
Monocarboxylate Transporter 1 Deficiency MNC019
Monoclonal Gammopathy of Uncertain Significance MNC006
Monoclonal Mast Cell Activation Syndrome MNC020
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
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
Monosomy 9q22.3 MNS011
Monostotic Fibrous Dysplasia MNS012
Montefiore Syndrome MNT045
Mood Disorder MDD011
Mooren's Ulcer MRN002
Morbid Obesity and Spermatogenic Failure MRB006
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
Mosaic Variegated Aneuploidy Syndrome 2 MSC106
Mosaic Variegated Aneuploidy Syndrome 3 MSC139
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
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
Moyamoya Disease 1 MYM013
Moyamoya Disease 2 MYM004
Moyamoya Disease 3 MYM005
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism MYM012
Moyamoya Disease 5 MYM003
Moyamoya Disease 6 with or Without Achalasia MYM015
Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome MPV001
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
Mucocele of Appendix MCC004
Mucocele of Salivary Gland MCC003
Mucocutaneous Leishmaniasis MCC002
Mucocutaneous Ulceration, Chronic MCC013
Mucoepidermoid Carcinoma MCP006
Mucoepidermoid Esophageal Carcinoma MCP008
Mucoepidermoid Thyroid Carcinoma MCP007
Mucoepithelial Dysplasia, Hereditary MCP039
Mucolipidoses MCL022
Mucolipidosis MCL001
Mucolipidosis Ii Alpha/beta MCL062
Mucolipidosis Iii Alpha/beta MCL046
Mucolipidosis Iii Gamma MCL016
Mucolipidosis Iv MCL013
Mucopolysaccharidoses MCP033
Mucopolysaccharidoses, Unclassified Types MCP042
Mucopolysaccharidosis Iii MCP001
Mucopolysaccharidosis Iv MCP004
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
Mucopolysaccharidosis, Type Iiia MCP043
Mucopolysaccharidosis, Type Iiib MCP044
Mucopolysaccharidosis, Type Iiic MCP045
Mucopolysaccharidosis, Type Iiid MCP046
Mucopolysaccharidosis, Type Iva MCP047
Mucopolysaccharidosis, Type Ivb MCP048
Mucopolysaccharidosis, Type Ix MCP051
Mucopolysaccharidosis, Type Vi MCP052
Mucopolysaccharidosis, Type Vii MCP049
Mucopolysaccharidosis-Plus Syndrome MCP040
Mucormycosis MCR141
Mucosal Melanoma MCS004
Mucositis MCS002
Mucus Inspissation of Respiratory Tract MCS005
Muenke Syndrome MNK003
Muir-Torre Syndrome MRT001
Mulchandani-Bhoj-Conlin Syndrome MLC004
Mulibrey Nanism MLB001
Muller Barth Menger Syndrome MLL007
Mullerian Aplasia MLL009
Mullerian Aplasia and Hyperandrogenism MLL011
Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly MLL022
Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies MLL021
Multicentric Carpotarsal Osteolysis Syndrome MLT092
Multicentric Castleman Disease MLT113
Multicentric Osteolysis Nephropathy MLT033
Multicentric Osteolysis, Nodulosis, and Arthropathy MLT065
Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum MLT138
Multicentric Papillary Thyroid Carcinoma MLT005
Multicentric Reticulohistiocytosis MLT016
Multicore Disease MLT168
Multicore Myopathy with Mental Retardation, Short Stature, and Hypogonadotropic Hypogonadism MLT146
Multicystic Dysplastic Kidney MLT084
Multidrug-Resistant Tuberculosis MLT006
Multifocal Atrial Tachycardia MLT131
Multifocal Choroiditis MLT035
Multifocal Dystonia MLT132
Multifocal Lymphangioendotheliomatosis with Thrombocytopenia MLT037
Multifocal Motor Neuropathy MLT075
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
Multiloculated Renal Cyst MLT112
Multiminicore Disease MLT028
Multinodular Goiter MLT008
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly MLT161
Multiple Acyl-Coa Dehydrogenase Deficiency MLT118
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
Multiple Carboxylase Deficiency MLT018
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
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 MLT128
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 MLT127
Multiple Cranial Nerve Palsy MLT009
Multiple Enchondromatosis, Maffucci Type MLT145
Multiple Endocrine Neoplasia MLT074
Multiple Endocrine Neoplasia, Type I MLT156
Multiple Endocrine Neoplasia, Type Iia MLT160
Multiple Endocrine Neoplasia, Type Iib MLT159
Multiple Endocrine Neoplasia, Type Iv MLT086
Multiple Epiphyseal Dysplasia MLT007
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
Multiple Exostoses with Spastic Tetraparesis MLT158
Multiple Familial Trichoepithelioma MLT048
Multiple Fibroadenomas of the Breast MLT120
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
Multiple Mitochondrial Dysfunctions Syndrome MLT027
Multiple Mitochondrial Dysfunctions Syndrome 1 MLT068
Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia MLT150
Multiple Mitochondrial Dysfunctions Syndrome 3 MLT119
Multiple Mitochondrial Dysfunctions Syndrome 4 MLT139
Multiple Mitochondrial Dysfunctions Syndrome 5 MLT151
Multiple Mitochondrial Dysfunctions Syndrome 6 MLT167
Multiple Mucosal Neuroma MLT011
Multiple Paragangliomas Associated with Polycythemia MLT106
Multiple Personality Disorder MLT010
Multiple Pterygium Syndrome, Escobar Variant MLT163
Multiple Pterygium Syndrome, Lethal Type MLT134
Multiple Pterygium Syndrome, X-Linked MLT148
Multiple Respiratory Chain Enzyme Deficiencies MLT057
Multiple Sclerosis MLT020
Multiple Sclerosis 2 MLT093
Multiple Sclerosis 3 MLT094
Multiple Sclerosis 4 MLT095
Multiple Sclerosis 5 MLT124
Multiple Sclerosis-Ichthyosis-Factor Viii Deficiency Syndrome MLT143
Multiple Self-Healing Squamous Epithelioma MLT152
Multiple Skull Base Meningioma MLT004
Multiple Spinal Canal and Spinal Cord Meningioma MLT014
Multiple Sulfatase Deficiency MLT135
Multiple Synostoses Syndrome MLT072
Multiple Synostoses Syndrome 1 MLT059
Multiple Synostoses Syndrome 2 MLT060
Multiple Synostoses Syndrome 3 MLT078
Multiple Synostoses Syndrome 4 MLT166
Multiple System Atrophy 1 MLT157
Multiple System Atrophy with Orthostatic Hypotension MLT076
Multiple System Atrophy, Cerebellar Type MLT105
Multiple System Atrophy, Parkinsonian Type MLT116
Multisystemic Smooth Muscle Dysfunction Syndrome MLT073
Mumps MMP001
Munchausen by Proxy MNC002
Mungan Syndrome MNG003
Murcs Association MRC004
Murray Valley Encephalitis MRR003
Muscle Cancer MSC072
Muscle Cramps, Familial MSC143
Muscle Disorders MSC033
Muscle Eye Brain Disease MSC077
Muscle Hypertrophy MSC007
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
Muscular Dystrophy, Barnes Type MSC145
Muscular Dystrophy, Becker Type MSC152
Muscular Dystrophy, Cardiac Type MSC153
Muscular Dystrophy, Congenital Merosin-Deficient, 1a MSC162
Muscular Dystrophy, Congenital, 1b MSC050
Muscular Dystrophy, Congenital, Davignon-Chauveau Type MSC141
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency MSC164
Muscular Dystrophy, Congenital, Lmna-Related MSC165
Muscular Dystrophy, Congenital, Megaconial Type MSC028
Muscular Dystrophy, Congenital, Merosin-Positive MSC029
Muscular Dystrophy, Congenital, Producing Arthrogryposis MSC131
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability MSC142
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
Muscular Dystrophy, Duchenne Type MSC157
Muscular Dystrophy, Hemizygous Lethal Type MSC154
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 MSC175
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2 MSC178
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 MSC180
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 4 MSC187
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 MSC169
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 MSC179
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 12 MSC181
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 17 MSC183
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 18 MSC184
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 MSC170
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 21 MSC186
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 23 MSC189
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 25 MSC191
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 MSC177
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 MSC176
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 MSC171
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 MSC173
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7 MSC174
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 MSC172
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
Muscular Dystrophy-Dystroglycanopathy , Type a, 10 MSC107
Muscular Dystrophy-Dystroglycanopathy , Type a, 11 MSC167
Muscular Dystrophy-Dystroglycanopathy , Type a, 12 MSC102
Muscular Dystrophy-Dystroglycanopathy , Type a, 13 MSC105
Muscular Dystrophy-Dystroglycanopathy , Type a, 14 MSC097
Muscular Dystrophy-Dystroglycanopathy , Type a, 2 MSC043
Muscular Dystrophy-Dystroglycanopathy , Type a, 3 MSC045
Muscular Dystrophy-Dystroglycanopathy , Type a, 4 MSC037
Muscular Dystrophy-Dystroglycanopathy , Type a, 5 MSC034
Muscular Dystrophy-Dystroglycanopathy , Type a, 6 MSC041
Muscular Dystrophy-Dystroglycanopathy , Type a, 7 MSC101
Muscular Dystrophy-Dystroglycanopathy , Type a, 8 MSC166
Muscular Dystrophy-Dystroglycanopathy , Type a, 9 MSC127
Muscular Dystrophy-Dystroglycanopathy , Type B, 1 MSC048
Muscular Dystrophy-Dystroglycanopathy , Type B, 14 MSC099
Muscular Dystrophy-Dystroglycanopathy , Type B, 2 MSC044
Muscular Dystrophy-Dystroglycanopathy , Type B, 3 MSC046
Muscular Dystrophy-Dystroglycanopathy , Type B, 4 MSC038
Muscular Dystrophy-Dystroglycanopathy , Type B, 5 MSC035
Muscular Dystrophy-Dystroglycanopathy , Type B, 6 MSC042
Muscular Dystrophy-Dystroglycanopathy , Type C, 1 MSC104
Muscular Dystrophy-Dystroglycanopathy , Type C, 12 MSC118
Muscular Dystrophy-Dystroglycanopathy , Type C, 14 MSC098
Muscular Dystrophy-Dystroglycanopathy , Type C, 15 MSC182
Muscular Dystrophy-Dystroglycanopathy , Type C, 2 MSC108
Muscular Dystrophy-Dystroglycanopathy , Type C, 3 MSC093
Muscular Dystrophy-Dystroglycanopathy , Type C, 4 MSC103
Muscular Dystrophy-Dystroglycanopathy , Type C, 5 MSC036
Muscular Dystrophy-Dystroglycanopathy , Type C, 7 MSC111
Muscular Dystrophy-Dystroglycanopathy , Type C, 8 MSC188
Muscular Dystrophy-Dystroglycanopathy , Type C, 9 MSC100
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
Mushroom Workers' Lung MSH001
Musical Aptitude Quantitative Trait Locus MSC163
Musical Perfect Pitch MSC148
Musk, Inability to Smell MSK002
Mutagen Sensitivity MTG002
Mutism MTS001
Mutyh-Associated Polyposis MTY001
Myalgia-Eosinophilia Syndrome Associated with Tryptophan MYL051
Myasthenia Gravis MYS003
Myasthenia Gravis Congenital MYS011
Myasthenia Gravis with Thymus Hyperplasia MYS007
Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors MYS072
Myasthenia, Limb-Girdle, Autoimmune MYS071
Myasthenic Syndrome, Congenital, 10 MYS052
Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency MYS057
Myasthenic Syndrome, Congenital, 12 MYS074
Myasthenic Syndrome, Congenital, 13 MYS075
Myasthenic Syndrome, Congenital, 14 MYS078
Myasthenic Syndrome, Congenital, 15 MYS077
Myasthenic Syndrome, Congenital, 16 MYS064
Myasthenic Syndrome, Congenital, 17 MYS056
Myasthenic Syndrome, Congenital, 18 MYS065
Myasthenic Syndrome, Congenital, 19 MYS070
Myasthenic Syndrome, Congenital, 1a, Slow-Channel MYS046
Myasthenic Syndrome, Congenital, 1b, Fast-Channel MYS047
Myasthenic Syndrome, Congenital, 20, Presynaptic MYS068
Myasthenic Syndrome, Congenital, 21, Presynaptic MYS069
Myasthenic Syndrome, Congenital, 22 MYS067
Myasthenic Syndrome, Congenital, 23, Presynaptic MYS080
Myasthenic Syndrome, Congenital, 24, Presynaptic MYS081
Myasthenic Syndrome, Congenital, 25, Presynaptic MYS082
Myasthenic Syndrome, Congenital, 2a, Slow-Channel MYS062
Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency MYS063
Myasthenic Syndrome, Congenital, 3a, Slow-Channel MYS048
Myasthenic Syndrome, Congenital, 3b, Fast-Channel MYS049
Myasthenic Syndrome, Congenital, 3c, Associated with Acetylcholine Receptor Deficiency MYS050
Myasthenic Syndrome, Congenital, 4a, Slow-Channel MYS059
Myasthenic Syndrome, Congenital, 4b, Fast-Channel MYS060
Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency MYS061
Myasthenic Syndrome, Congenital, 5 MYS051
Myasthenic Syndrome, Congenital, 6, Presynaptic MYS055
Myasthenic Syndrome, Congenital, 7, Presynaptic MYS044
Myasthenic Syndrome, Congenital, 8 MYS076
Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency MYS054
Mybpc1-Related Autosomal Recessive Non-Lethal Arthrogryposis Multiplex Congenita Syndrome MYB004
Mycetoma MYC012
Mycobacterium Abscessus MYC013
Mycobacterium Avium Complex Infections MYC088
Mycobacterium Chelonae MYC014
Mycobacterium Fortuitum MYC015
Mycobacterium Gordonae MYC016
Mycobacterium Kansasii MYC017
Mycobacterium Malmoense MYC018
Mycobacterium Marinum MYC019
Mycobacterium Tuberculosis 1 MYC084
Mycobacterium Tuberculosis 2 MYC054
Mycobacterium Tuberculosis 3 MYC055
Mycobacterium Tuberculosis X-Linked MYC081
Mycobacterium Tuberculosis, Susceptibility to Infection by MYC020
Mycobacterium Xenopi MYC021
Mycophenolate Mofetil Embryopathy MYC060
Mycoplasma Encephalitis MYC062
Mycoplasma Pneumoniae Pneumonia MYC087
Mycosis Fungoides MYC006
Mycotic Corneal Ulcer MYC004
Myd88 Deficiency MYD002
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
Myelodysplastic Syndrome with Excess Blasts MYL074
Myelofibrosis MYL005
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 Pdgfrb Rearrangement MYL065
Myelolymphatic Insufficiency MYL071
Myeloma, Multiple MYL069
Myelomeningocele MYL020
Myelopathy, Htlv-1-Associated MYL057
Myeloperoxidase Deficiency MYL013
Myelophthisic Anemia MYL002
Myeloproliferative Disease, Autosomal Recessive MYL070
Myeloproliferative Disorder, Chronic, with Eosinophilia MYL067
Myeloproliferative Neoplasm MYL031
Myeloproliferative Syndrome, Transient MYL058
Myeloproliferative/lymphoproliferative Neoplasms, Familial MYL064
Myh-9 Related Disease MYH015
Myh9 Related Thrombocytopenia MYH004
Myhre Syndrome MYH012
Myiasis MYS004
Myo5b-Related Progressive Familial Intrahepatic Cholestasis MY5001
Myoblastoma MYB001
Myocardial Infarction MYC007
Myocardial Infarction 2 MYC058
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
Myoclonic Epilepsy in Non-Progressive Encephalopathies MYC061
Myoclonic Epilepsy Myopathy Sensory Ataxia MYC030
Myoclonic Epilepsy of Infancy MYC068
Myoclonic Epilepsy of Lafora MYC079
Myoclonic Epilepsy of Unverricht and Lundborg MYC080
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders MYC082
Myoclonic Epilepsy, Familial Infantile MYC083
Myoclonic Epilepsy, Hartung Type MYC077
Myoclonic Epilepsy, Juvenile 3 MYC085
Myoclonic Epilepsy, Juvenile 4 MYC086
Myoclonic-Astastic Epilepsy MYC069
Myoclonic-Atonic Epilepsy MYC071
Myoclonus MYC033
Myoclonus and Ataxia MYC078
Myoclonus Epilepsy MYC026
Myoclonus Epilepsy Partial Seizure MYC027
Myoclonus, Cerebellar Ataxia, and Deafness MYC074
Myoclonus, Familial, 1 MYC089
Myoclonus, Familial, 2 MYC090
Myoclonus, Intractable, Neonatal MYC075
Myoepithelial Carcinoma MYP002
Myoepithelioma MYP001
Myofascial Pain Syndrome MYF002
Myofibrillar Lysis MYF004
Myofibrillar Myopathy MYF003
Myofibroma MYF001
Myofibromatosis, Infantile, 1 MYF007
Myofibromatosis, Infantile, 2 MYF010
Myoglobinuria MYG005
Myoglobinuria Dominant Form MYG002
Myoglobinuria, Acute Recurrent, Autosomal Recessive MYG004
Myoglobinuria, Autosomal Dominant MYG006
Myoglobinuria, Recurrent MYG007
Myokymia with Neonatal Epilepsy MYK001
Myoma MYM001
Myopathic Intestinal Pseudoobstruction MYP066
Myopathy MYP004
Myopathy - Thyrotoxic MYP026
Myopathy Due to Malate-Aspartate Shuttle Defect MYP129
Myopathy Due to Myoadenylate Deaminase Deficiency MYP071
Myopathy Mitochondrial Cataract MYP014
Myopathy of Extraocular Muscle MYP005
Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme MYP025
Myopathy with Deficiency of Iscu MYP009
Myopathy with Extrapyramidal Signs MYP086
Myopathy with Giant Abnormal Mitochondria MYP130
Myopathy with Hexagonally Cross-Linked Tubular Arrays MYP061
Myopathy with Lactic Acidosis, Hereditary MYP097
Myopathy with Storage of Glycoproteins and Glycosaminoglycans MYP126
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset MYP093
Myopathy, Autophagic Vacuolar, Infantile-Onset MYP142
Myopathy, Autosomal Recessive, with Rigid Spine and Distal Joint Contractures MYP152
Myopathy, Centronuclear, 1 MYP123
Myopathy, Centronuclear, 2 MYP131
Myopathy, Centronuclear, 4 MYP098
Myopathy, Centronuclear, 5 MYP148
Myopathy, Centronuclear, 6, with Fiber-Type Disproportion MYP150
Myopathy, Centronuclear, X-Linked MYP136
Myopathy, Congenital MYP132
Myopathy, Congenital, Bailey-Bloch MYP151
Myopathy, Congenital, Compton-North MYP038
Myopathy, Congenital, with Fast-Twitch Fiber Atrophy MYP154
Myopathy, Congenital, with Fiber-Type Disproportion MYP091
Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked MYP039
Myopathy, Distal, 1 MYP125
Myopathy, Distal, 3 MYP112
Myopathy, Distal, 4 MYP095
Myopathy, Distal, 5 MYP116
Myopathy, Distal, Infantile-Onset MYP124
Myopathy, Distal, Tateyama Type MYP067
Myopathy, Distal, with Anterior Tibial Onset MYP035
Myopathy, Distal, with Rimmed Vacuoles MYP120
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia MYP128
Myopathy, Isolated Mitochondrial, Autosomal Dominant MYP099
Myopathy, Lactic Acidosis, and Sideroblastic Anemia MYP108
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 MYP021
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 MYP022
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 MYP107
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay MYP017
Myopathy, Mitochondrial, and Ataxia MYP149
Myopathy, Myofibrillar, 1 MYP072
Myopathy, Myofibrillar, 2 MYP082
Myopathy, Myofibrillar, 3 MYP078
Myopathy, Myofibrillar, 4 MYP080
Myopathy, Myofibrillar, 5 MYP079
Myopathy, Myofibrillar, 6 MYP081
Myopathy, Myofibrillar, 7 MYP119
Myopathy, Myofibrillar, 8 MYP118
Myopathy, Myofibrillar, 9, with Early Respiratory Failure MYP153
Myopathy, Myofibrillar, Fatal Infantile Hypertonic, Alpha-B Crystallin-Related MYP121
Myopathy, Myosin Storage, Autosomal Dominant MYP105
Myopathy, Myosin Storage, Autosomal Recessive MYP106
Myopathy, Proximal, and Ophthalmoplegia MYP139
Myopathy, Scapulohumeroperoneal MYP114
Myopathy, Spheroid Body MYP094
Myopathy, Tubular Aggregate, 1 MYP087
Myopathy, Tubular Aggregate, 2 MYP088
Myopathy, Vacuolar, with Casq1 Aggregates MYP104
Myopathy, X-Linked, with Excessive Autophagy MYP100
Myopathy, X-Linked, with Postural Muscle Atrophy MYP056
Myopathy-Growth Delay-Intellectual Disability-Hypospadias Syndrome MYP110
Myopericytoma MYP064
Myopia MYP006
Myopia 1, X-Linked MYP137
Myopia 10 MYP044
Myopia 11, Autosomal Dominant MYP143
Myopia 12, Autosomal Dominant MYP144
Myopia 13, X-Linked MYP134
Myopia 14 MYP069
Myopia 15, Autosomal Dominant MYP146
Myopia 16, Autosomal Dominant MYP145
Myopia 17, Autosomal Dominant MYP140
Myopia 18, Autosomal Recessive MYP133
Myopia 19, Autosomal Dominant MYP147
Myopia 2, Autosomal Dominant MYP127
Myopia 20, Autosomal Dominant MYP084
Myopia 21, Autosomal Dominant MYP070
Myopia 22, Autosomal Dominant MYP075
Myopia 23, Autosomal Recessive MYP074
Myopia 24, Autosomal Dominant MYP090
Myopia 25, Autosomal Dominant MYP117
Myopia 26, X-Linked, Female-Limited MYP135
Myopia 3, Autosomal Dominant MYP138
Myopia 5, Autosomal Dominant MYP141
Myopia 6 MYP018
Myopia 7 MYP040
Myopia 8 MYP041
Myopia 9 MYP048
Myopia, High, with Cataract and Vitreoretinal Degeneration MYP073
Myopic Macular Degeneration MYP060
Myosclerosis, Autosomal Recessive MYS016
Myosin Storage Myopathy MYS032
Myosinopathies MYS066
Myositis MYS005
Myositis Fibrosa MYS002
Myositis Ossificans MYS001
Myospherulosis MYS028
Myostatin-Related Muscle Hypertrophy MYS010
Myotonia MYT011
Myotonia Atrophica MYT026
Myotonia Congenita MYT023
Myotonia Congenita, Autosomal Dominant MYT027
Myotonia Congenita, Autosomal Recessive MYT029
Myotonia with Skeletal Abnormalities and Mental Retardation MYT024
Myotonia, Potassium-Aggravated MYT030
Myotonic Cataract MYT001
Myotonic Disease MYT003
Myotonic Dystrophy MYT002
Myotonic Dystrophy 1 MYT021
Myotonic Dystrophy 2 MYT020
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
Myxoid Liposarcoma of the Ovary MYX002
Myxoma, Intracardiac MYX012
Myxomatous Pattern Testicular Yolk Sac Tumor MYX003
Myxopapillary Ependymoma MYX001
Myxosarcoma MYX007
Myxozoa MYX011
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