Disease Name Symbol Acronym
Machado-Joseph Disease MCH002 SCA3
Machado-Joseph Disease Type 1 MCH012
Machado-Joseph Disease Type 2 MCH014
Machado-Joseph Disease Type 3 MCH013
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies MCR021 AGBK
Macrocephaly-Intellectual Disability-Neurodevelopmental Disorder-Small Thorax Syndrome MCR313
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis MCR095 MACS
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation MCR321 MDFPMR
Macrocephaly, Macrosomia, Facial Dysmorphism Syndrome MCR221 MMFD
Macrocephaly/autism Syndrome MCR096 MCEPHAS
Macrocephaly/megalencephaly Syndrome, Autosomal Recessive MCR237 MGCPH
Macrocytic Anemia MCR017
Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic MCR128 MAR
Macrodactyly of Fingers MCR184
Macrodactyly of Fingers, Unilateral MCR188
Macrodactyly of Toes MCR185
Macrodactyly of Toes, Unilateral MCR190
Macroglobulinemia MCR004
Macroglobulinemia, Waldenstrom 1 MCR161
Macroglobulinemia, Waldenstrom 2 MCR162
Macroglossia MCR037
Macrophage Activation Syndrome MCR225
Macrophthalmia, Colobomatous, with Microcornea MCR317
Macrostomia, Isolated MCR302
Macrothrombocytopenia and Progressive Sensorineural Deafness MCR139 MPSD
Macrothrombocytopenia Progressive Deafness MCR041
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related MCR125 MAD-TUBB1
Macrozoospermia MCR265 SPGF5
Macular Amyloidosis MCL047
Macular Corneal Dystrophy MCL002 MCD
Macular Degeneration, Age-Related 5 MCL064 ARMD5
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, Reduced Risk of MCL054 ARMD14
Macular Degeneration, Age-Related, 15 MCL065 ARMD15
Macular Degeneration, Age-Related, 2 MCL043 ARMD2
Macular Degeneration, Age-Related, 3 MCL040 ARMD3
Macular Degeneration, Age-Related, 4 MCL038 ARMD4
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, Butterfly-Shaped Pigmentary, 2 MCL063 MDPT2
Macular Dystrophy, Concentric Annular MCL018 MCDCA
Macular Dystrophy, Dominant Cystoid MCL027 DCMD
Macular Dystrophy, Patterned, 1 MCL059 MDPT1
Macular Dystrophy, Retinal, 1, North Carolina Type MCL069 NCMD
Macular Dystrophy, Retinal, 2 MCL035 MCDR2
Macular Dystrophy, Retinal, 3 MCL026
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 Holes MCL003
Macular Retinal Edema MCL006
Madelung Deformity MDL024
Madras Motor Neuron Disease MDR004 MMND
Magi2-Related Infantile Spasms MG2001
Main Bronchus Cancer MNB001
Majeed Syndrome MJD001 MJDS
Major Affective Disorder 1 MJR007
Major Affective Disorder 2 MJR008
Major Affective Disorder 4 MJR004
Major Affective Disorder 5 MJR006
Major Affective Disorder 6 MJR003
Major Affective Disorder-7 MJR018 MAFD7
Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment MJR011 MDD
Mak-Related Retinitis Pigmentosa MKR001 RP62
Malaria MLR004 CM
Malaria, Mild MLR020
Male Infertility MLN007
Male Reproductive Organ Benign Neoplasm MLR005
Male Reproductive Organ Cancer MLR006
Male Reproductive System Disease MLR007
Maligant Granulosa Cell Tumor of Ovary MLG129
Malignant Anus Melanoma MLG038
Malignant Atrophic Papulosis MLG141
Malignant Biphasic Mesothelioma MLG011
Malignant Choroid Melanoma MLG061
Malignant Ciliary Body Melanoma MLG062
Malignant Conjunctival Melanoma MLG142
Malignant Cylindroma MLG087
Malignant Dermis Tumor MLG063
Malignant Ectomesenchymoma MLG133
Malignant Ependymoma MLG064
Malignant Epithelial Mesothelioma MLG012
Malignant Epithelial Tumor of Salivary Glands MLG134
Malignant Essential Hypertension MLG039
Malignant Fibrous Histiocytoma of Bone MLG014
Malignant Fibroxanthoma MLG065 MFH
Malignant Germ Cell Tumor MLG088
Malignant Giant Cell Tumor MLG067
Malignant Giant Cell Tumor of Soft Parts MLG018
Malignant Glandular Tumor of Peripheral Nerve Sheath MLG051
Malignant Glioma MLG068
Malignant Granular Cell Myoblastoma MLG032
Malignant Histiocytosis MLG054
Malignant Hypertension MLG069
Malignant Hyperthermia MLG056 MH
Malignant Hyperthermia of Anesthesia MLG143
Malignant Hyperthermia Susceptibility MLG086
Malignant Hyperthermia Susceptibility 1 MLG132 MHS1
Malignant Hyperthermia Susceptibility 5 MLG131 MHS5
Malignant Iris Melanoma MLG070
Malignant Leptomeningeal Tumor MLG071
Malignant Leydig Cell Tumor MLG072
Malignant Melanoma, Somatic MLG108 CMM
Malignant Mesenchymoma MLG074
Malignant Migrating Partial Seizures of Infancy MLG120 MPEI
Malignant Mixed Mullerian Tumor MLG098 MMMT
Malignant Otitis Externa MLG042
Malignant Ovarian Brenner Tumor MLG053
Malignant Ovarian Cyst MLG033
Malignant Ovarian Surface Epithelial-Stromal Neoplasm MLG076
Malignant Peripheral Nerve Sheath Tumor MLG077 MPNST
Malignant Peritoneal Mesothelioma MLG002
Malignant Pineal Area Germ Cell Neoplasm MLG078
Malignant Pleural Mesothelioma MLG079
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 Ovary MLG128
Malignant Skin Fibrous Histiocytoma MLG007
Malignant Spindle Cell Melanoma MLG005
Malignant Spiradenoma MLG036 MES
Malignant Struma Ovarii MLG059
Malignant Syringoma MLG049
Malignant Teratoma MLG081
Malignant Triton Tumor MLG041 MTT
Malonyl-Coa Decarboxylase Deficiency MLN011 MLYCD DEFICIENCY
Malouf Syndrome MLF002 CMDHH
Mammary Paget's Disease MMM001
Mammary-Digital-Nail Syndrome MMM002
Man1b1-Cdg MN1002
Mandibular Cancer MND001
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome MND021 MDPL
Mandibuloacral Dysplasia MND007 MADA
Mandibuloacral Dysplasia with Type B Lipodystrophy MND002 MADB
Mandibulofacial Dysostosis with Alopecia MND025 MFDA
Mandibulofacial Dysostosis, Guion-Almeida Type MND020 MFDM
Manitoba Oculotrichoanal Syndrome MNT006 MOTA
Mannosidosis MNN018
Mannosidosis, Alpha-, Types I and Ii MNN025 MANSA
Mannosidosis, Beta MNN044 MANSB
Mansonelliasis MNS001
Mantle Cell Lymphoma MNT001 LCM
Maoa-Related Behavior Disorders MRL005
Map2k1-Related Cardiofaciocutaneous Syndrome MP2001
Map2k1-Related Noonan Syndrome MP2002
Map2k2-Related Cardiofaciocutaneous Syndrome MP2003
Map3k1-Related 46,xy Dsd and 46,xy Cgd MP3001 SRXY6
Maple Syrup Urine Disease, Mild Variant MPL011 MSUDMV
Maple Syrup Urine Disease, Type Ii MPL012 MSUD
Mapt-Related Disorders MPT001
Marantic Endocarditis MRN001
Marasmus MRS001
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
Marginal Zone B-Cell Lymphoma MRG003 MZL
Marie Unna Congenital Hypotrichosis MRN005 MUHH
Marinesco-Sjogren Syndrome MRN003 MSS
Marshall Syndrome MRS002 MRSHS
Marshall-Smith Syndrome MRS004 MRSHSS
Martsolf Syndrome MRT007 MARTS
Masa Syndrome MSS001 SPG1
Masp2 Deficiency MSP001 MASPD
Mass Syndrome MSS002 OCTD
Mast Cell Activation Syndrome MST020 MCAS
Mast Cell Disease MST017
Mast Cell Neoplasm MST004
Mast Syndrome MST006 SPG21
Mast-Cell Leukemia MST002
Mast-Cell Sarcoma MST001
Masters-Allen Syndrome MST003
Mastitis MST005
Mastl-Related Thrombocytopenia 2 MST015
Mastocytosis MST009
Mastoiditis MST019
Maternal 14q32.2 Hypermethylation Syndrome MTR056
Maternal 14q32.2 Microdeletion Syndrome MTR055
Maternal Uniparental Disomy of Chromosome 1 MTR051
Maternal Uniparental Disomy of Chromosome 16 MTR067
Maternally-Inherited Cardiomyopathy and Hearing Loss MTR049
Maternally-Inherited Progressive External Ophthalmoplegia MTR058
Maternally-Inherited Spastic Paraplegia MTR059
Mature B-Cell Neoplasm MTR008
Mature Cataract MTR001
Mature Teratoma MTR010
Mature Teratoma of the Ovary MTR011
Maturity-Onset Diabetes of the Young MTR004 MODY
Maturity-Onset Diabetes of the Young 6 MTR071 MODY6
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 Ix MTR072 MODY9
Maturity-Onset Diabetes of the Young, Type Vii MTR070 MODY7
Maturity-Onset Diabetes of the Young, Type Viii MTR073 MODY8
Max-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome MXR002
Max-Related Susceptibility to Pheochromocytoma MXR001
Maxillary Sinus Adenoid Cystic Carcinoma MXL002
Maxillary Sinus Cancer MXL008
Maxillary Sinus Squamous Cell Carcinoma MXL004
Maxillary Sinusitis MXL015
Maxillonasal Dysplasia, Binder Type MXL016
May-Hegglin Anomaly MYH001 MHA
May-Thurner Syndrome MYT019
Mayer-Rokitansky-Kuster-Hauser Syndrome MYR002 RKH SYNDROME
Mazabraud Syndrome MZB001
Mbd5 Haploinsufficiency MBD001 MAND
Mcardle Disease MCR264 GSD5
Mccc1-Related 3-Methylcrotonyl-Coa Carboxylase Deficiency MCC007
Mccc2-Related 3-Methylcrotonyl-Coa Carboxylase Deficiency MCC008
Mccune-Albright Syndrome, Somatic, Mosaic MCC010 MAS
Mcee-Related Methylmalonic Acidemia MCR097
Mckusick-Kaufman Syndrome MCK005 MKKS
Mcleod Neuroacanthocytosis Syndrome MCL014
Mcleod Syndrome with or Without Chronic Granulomatous Disease MCL055 MLS
Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency MCT002
Meacham Syndrome MCH011 MEACHS
Measles MSL001
Mechanical Ectropion MCH001
Mechanical Strabismus MCH006
Meckel Syndrome 1 MCK022 MKS1
Meckel Syndrome 10 MCK023 MKS10
Meckel Syndrome 11 MCK027 MKS11
Meckel Syndrome 12 MCK026 MKS12
Meckel Syndrome 2 MCK025 MKS2
Meckel Syndrome 3 MCK024 MKS3
Meckel Syndrome 4 MCK017 MKS4
Meckel Syndrome 5 MCK019 MKS5
Meckel Syndrome 6 MCK016 MKS6
Meckel Syndrome 7 MCK015 MKS7
Meckel Syndrome 8 MCK018 MKS8
Meckel Syndrome 9 MCK021 MKS9
Meckel's Diverticulum MCK002
Meconium Aspiration Syndrome MCN007 MAS
Meconium Ileus MCN017 MECIL
Mecp2-Related Angelman-Like Syndrome MCP021
Mecp2-Related Disorders MCP017
Mecp2-Related Severe Neonatal Encephalopathy MCP022
Med12-Related Disorders MD1001
Med13l Syndrome MD1002
Med23 MD2001 MED23
Median Arcuate Ligament Syndrome MDN008 MALS
Median Neuropathy MDN002
Median Rhomboid Glossitis MDN001
Mediastinal Cancer MDS018
Mediastinal Gray Zone Lymphoma MDS006
Mediastinal Lipomatosis MDS003
Mediastinal Malignant Lymphoma MDS019
Mediastinitis MDS022
Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency MDM001 MCADD
Mednik Syndrome MDN005 MEDNIK
Medullary Cystic Kidney Disease 1 MDL008 MCKD1
Medullary Cystic Kidney Disease 2 MDL021 MCKD2
Medullary Sponge Kidney MDL009 MSK
Medullary Thyroid Carcinoma, Familial MDL022 MTC
Medulloblastoma MDL005 MDB
Medulloblastoma, Ptch2-Related MDL025 MDB
Medulloblastoma, Sufu-Related MDL011
Medulloepithelioma MDL002
Medullomyoblastoma MDL003
Meesmann Corneal Dystrophy MSM001 MECD
Mef2a-Related Coronary Artery Disease Susceptibility MF2001
Megacolon MGC001
Megaesophagus MGS001
Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) MGK005
Megakaryocytic Leukemia MGK001 AMKL
Megalencephalic Leukoencephalopathy with Subcortical Cysts MGL002 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-Capillary Malformation-Polymicrogyria Syndrome, Somatic MGL023 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
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome, Somatic MGL024
Megalencephaly-Severe Kyphoscoliosis-Overgrowth Syndrome MGL034
Megaloblastic Anemia MGL001 IGS
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency MGL012 DHFRD
Megaloblastic Anemia-1, Finnish Type MGL016 RH-MGA1
Megalocornea MGL003
Megalocornea 1, X-Linked MGL026 MGC1
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
Meige Syndrome MGS004
Melancholia MLN003
Melanoacanthoma MLN005
Melanocytic Nevus Syndrome, Congenital, Somatic MLN054 CMNS
Melanoma MLN008
Melanoma and Neural System Tumor Syndrome MLN012 MASTS
Melanoma Metastasis MLN013
Melanoma of Soft Tissue MLN064
Melanoma-Associated Retinopathy MLN046
Melanoma, Cutaneous Malignant 10 MLN055 CMM10
Melanoma, Cutaneous Malignant 8 MLN043 CMM8
Melanoma, Cutaneous Malignant, 2 MLN032 CMM2
Melanoma, Cutaneous Malignant, 3 MLN050 CMM3
Melanoma, Cutaneous Malignant, 5 MLN052 CMM5
Melanoma, Cutaneous Malignant, 6 MLN051 CMM6
Melanoma, Cutaneous Malignant, 9 MLN049 CMM9
Melanoma, Uveal 1 MLN039
Melanoma, Uveal 2 MLN041
Melanomatosis MLN002
Melanotic Medulloblastoma MLN004
Melanotic Neurilemmoma MLN009
Melanotic Neuroectodermal Tumor MLN001
Melas, Mt-Nd1-Related MLS003
Melas, Mt-Nd5-Related MLS004
Melas, Mt-Nd6-Related MLS005
Melas, Mt-Tf-Related MLS006
Melas, Mt-Th-Related MLS012
Melas, Mt-Tk-Related MLS007
Melas, Mt-Tl1-Related MLS008
Melas, Mt-Tq-Related MLS009
Melas, Mt-Ts1-Related MLS010
Melas, Mt-Ts2-Related MLS011
Meleda Disease MLD003 MDM
Melioidosis MLD001
Melkersson-Rosenthal Syndrome MLK003 MRS
Melnick-Needles Syndrome MLN014 MNS
Melon Allergy MLN063
Melorheostosis MLR003
Melorheostosis with Osteopoikilosis MLR010 MEL
Membranoproliferative Glomerulonephritis MMB001 MPGN
Membranous Nephropathy MMB011 MGN
Mend Syndrome MND023 MEND
Meniere's Disease MNR002
Meningeal Melanocytoma MNN001
Meningeal Melanoma MNN010
Meningeal Melanomatosis MNN008
Meninges Hemangiopericytoma MNN006
Meninges Sarcoma MNN011
Meningioma, Familial MNN043 MNGMA
Meningioma, Familial Susceptibility MNN045
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
Mental Depression MNT002
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 Epilepsy MNT014
Mental Retardation with Language Impairment and Autistic Features MNT069
Mental Retardation with Language Impairment and with or Without Autistic Features MNT237 MRLIAF
Mental Retardation-Hypotonic Facies Syndrome, X-Linked MNT061 MRXSHF1
Mental Retardation, Anterior Maxillary Protrusion, and Strabismus MNT118 MRAMS
Mental Retardation, Autosomal Dominant 10 MNT186 MRD10
Mental Retardation, Autosomal Dominant 11 CHL091 MRD11
Mental Retardation, Autosomal Dominant 12 MNT164
Mental Retardation, Autosomal Dominant 13 MNT143 MRD13
Mental Retardation, Autosomal Dominant 14 MNT156 CSS2
Mental Retardation, Autosomal Dominant 15 MNT153 CSS3
Mental Retardation, Autosomal Dominant 16 MNT152 CSS4
Mental Retardation, Autosomal Dominant 17 MNT171 SHMS
Mental Retardation, Autosomal Dominant 18 MNT157 MRD18
Mental Retardation, Autosomal Dominant 19 MNT159 MRD19
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 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 37 MNT235 WHSUS
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 44 MNT273 MRD44
Mental Retardation, Autosomal Dominant 6 MNT144 MRD6
Mental Retardation, Autosomal Dominant 7 MNT185 MRD7
Mental Retardation, Autosomal Dominant 8 MNT168 MRD8
Mental Retardation, Autosomal Dominant, 27 MNT209 MRD27
Mental Retardation, Autosomal Recessive 14 MNT154 MRT14
Mental Retardation, Autosomal Recessive 15 MNT150 MRT15
Mental Retardation, Autosomal Recessive 16 MNT167
Mental Retardation, Autosomal Recessive 18 MNT151 MRT18
Mental Retardation, Autosomal Recessive 19 MNT182
Mental Retardation, Autosomal Recessive 2 MNT155 MRT2A
Mental Retardation, Autosomal Recessive 23 MNT170
Mental Retardation, Autosomal Recessive 24 MNT162
Mental Retardation, Autosomal Recessive 25 MNT172
Mental Retardation, Autosomal Recessive 27 MNT177 MRT27
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 32 MNT175
Mental Retardation, Autosomal Recessive 33 MNT180
Mental Retardation, Autosomal Recessive 34 MNT173 MRT34
Mental Retardation, Autosomal Recessive 35 MNT181
Mental Retardation, Autosomal Recessive 36 MNT183 MRT36
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, 37 MNT169 MRT37
Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity MNT038
Mental Retardation, Fra12a Type MNT107
Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations MNT053 MRD20
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis MNT112 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 104 MNT267 MRX104
Mental Retardation, X-Linked 105 MNT274 MRX105
Mental Retardation, X-Linked 12/35 MNT249 MRX12
Mental Retardation, X-Linked 23 MNT204
Mental Retardation, X-Linked 29 and Others MNT189 MRXARX
Mental Retardation, X-Linked 3 MNT149 MRX3
Mental Retardation, X-Linked 30/47 MNT203 MRX30
Mental Retardation, X-Linked 42 MNT205
Mental Retardation, X-Linked 49 MNT187 MRX49
Mental Retardation, X-Linked 50 MNT194
Mental Retardation, X-Linked 53 MNT202
Mental Retardation, X-Linked 61 MNT271 MRX61
Mental Retardation, X-Linked 73 MNT247
Mental Retardation, X-Linked 92 MNT196 MRX92
Mental Retardation, X-Linked 96 MNT195 MRX96
Mental Retardation, X-Linked 97 MNT200 MRXZ
Mental Retardation, X-Linked 98 MNT198 MRX98
Mental Retardation, X-Linked 99 MNT218 MRX99
Mental Retardation, X-Linked Syndromic 5 MNT230 PGS
Mental Retardation, X-Linked Syndromic, Christianson Type MNT121 MRXSCH
Mental Retardation, X-Linked Syndromic, Lubs Type MNT208 MRXSL
Mental Retardation, X-Linked Syndromic, Nascimento-Type MNT231 MRXSN
Mental Retardation, X-Linked Syndromic, Raymond Type MNT232 MRXSZ
Mental Retardation, X-Linked Syndromic, Turner Type MNT139 MRXST
Mental Retardation, X-Linked, Fraxe Type MNT068 MRFRAXE
Mental Retardation, X-Linked, Snyder-Robinson Type MNT054 MRXSSR
Mental Retardation, X-Linked, Syndromic 13 MNT135 MRXS13
Mental Retardation, X-Linked, Syndromic 15 MNT109 MRXS15
Mental Retardation, X-Linked, Syndromic 17 MNT191
Mental Retardation, X-Linked, Syndromic 32 MNT207 MRXS32
Mental Retardation, X-Linked, Syndromic 9 MNT197 MRXS9
Mental Retardation, X-Linked, Syndromic, 33 MNT265 MRXS33
Mental Retardation, X-Linked, Syndromic, Bain Type MNT269 MRXSB
Mental Retardation, X-Linked, Syndromic, Borck Type MNT268 MRXSBRK
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, Martin-Probst Type MNT146 MRXSMP
Mental Retardation, X-Linked, Syndromic, Wilson-Turner Type MNT260 WTS
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 Growth Hormone Deficiency MNT059 MRGH
Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency MNT119 MRXGH
Mental Retardation, X-Linked, with Short Stature, Small Testes, Muscle Wasting, and Tremor MNT060 MRXC
Mental Retsrdation, X-Linked Syndromic, Female Restricted MNT261
Mephenytoin Poor Metabolizer MPH001
Mercaptolactate-Cysteine Disulfiduria MRC009
Mercury Poisoning MRC003
Merkel Cell Carcinoma MRK001 MCC
Merrf/melas Overlap Syndrome MRR006
Mertk-Related Retinitis Pigmentosa MRT008 RP38
Mesangial Proliferative Glomerulonephritis MSN001
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
Mesocestoidiasis MSC001
Mesomelia MSM003
Mesomelia-Synostoses Syndrome MSM004
Mesomelic Dysplasia, Kantaputra Type MSM016 MDK
Mesomelic Dysplasia, Savarirayan Type MSM019
Mesothelioma, Somatic MST016 MESOM
Mesp2-Related Spondylocostal Dysostosis, Autosomal Recessive MSP002 SCDO2
Metabolic Acidosis MTB004
Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration MTB007 MECRCN
Metacarpal 4-5 Fusion MTC100 MF4
Metachondromatosis MTC018 MC
Metachromatic Leukodystrophy MTC003 MLD
Metachromatic Leukodystrophy Due to Sap-B Deficiency MTC067 MLD-SAPB
Metachromatic Leukodystrophy, Adult Form MTC074
Metachromatic Leukodystrophy, Juvenile Form MTC076
Metachromatic Leukodystrophy, Late Infantile Form MTC075
Metagonimiasis MTG001
Metal Allergy MTL005
Metal Metabolism Disorder MTL002
Metanephric Adenoma MTN001
Metaphyseal Anadysplasia MTP005 MAD
Metaphyseal Anadysplasia 2 MTP014 MANDP2
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa MTP031
Metaphyseal Chondrodysplasia, Murk Jansen Type MTP026 JMC
Metaphyseal Chondrodysplasia, Schmid Type MTP025 SMCD
Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly MTP023 MDMHB
Metaphyseal Dysplasia Without Hypotrichosis MTP003 CHHV
Metaphyseal Dysplasia, Spahr Type MTP028 MDST
Metaphyseal Enchondromatosis with D-2-Hydroxyglutaric Aciduria MTP033
Metaphyseal Undermodeling, Spondylar Dysplasia, and Overgrowth MTP011
Metatropic Dysplasia MTT002 MTD
Metatypical Basal Cell Carcinoma MTT001
Methanol Poisoning MTH047
Methemoglobinemia MTH007
Methemoglobinemia, Beta-Globin Type MTH064
Methemoglobinemia, Type I MTH037 METHB-CYB5R3
Methemoglobinemia, Type Iv MTH036 METHB-CYB5A
Methotrexate Toxicity or Dose Selection MTH061
Methylmalonate Semialdehyde Dehydrogenase Deficiency MTH013 MMSDHD
Methylmalonic Acidemia MTH008 MMA
Methylmalonic Acidemia with Homocystinuria MTH021
Methylmalonic Acidemia with Homocystinuria Type Cbld MTH066 CBLD
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 MMAHCC
Methylmalonic Aciduria and Homocystinuria, Cbld Type MTH055 MMAHCD
Methylmalonic Aciduria and Homocystinuria, Cblf Type MTH056 MMAHCF
Methylmalonic Aciduria and Homocystinuria, Cblj Type MTH051 MAHCJ
Methylmalonic Aciduria Due to Transcobalamin Receptor Defect MTH032 MMATC
Methylmalonic Aciduria, Mut(0) Type MTH039 MMAM
Methylmalonic Aciduria, Vitamin B12-Responsive MTH033 MMAA
Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type MTH034 MMAB
Methylmalonyl-Coa Epimerase Deficiency MTH040 MCEED
Methylmalonyl-Coenzyme a Mutase Deficiency MTH025
Mevalonic Aciduria MVL001 MEVA
Mfap5-Related Thoracic Aortic Aneurysms and Aortic Dissections MFP001 AAT9
Mgme1-Related Mitochondrial Dna Depletion Syndrome MGM001
Mhc Class Ii Deficiency MHC001 BLS 2
Michelin Tire Baby Syndrome MCH008
Microcephalic Osteodysplastic Primordial Dwarfism, Type I MCR240 TALS
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii MCR258 MOPD2
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 2, Primary, Autosomal Recessive, with or Without Cortical Malformations MCR222 MCPH2
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, Autosomal Recessive, 1 MCR259 MCCRP1
Microcephaly and Chorioretinopathy, Autosomal Recessive, 2 MCR244 MCCRP2
Microcephaly and Chorioretinopathy, Autosomal Recessive, 3 MCR272 MCCRP3
Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation MCR216 MCLMR
Microcephaly with Polymicrogyria MCR275
Microcephaly-Capillary Malformation Syndrome MCR183 MICCAP
Microcephaly-Complex Motor and Sensory Axonal Neuropathy Syndrome MCR298
Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome MCR285
Microcephaly, Amish Type MCR257 MCPHA
Microcephaly, Congenital Cataract and Psoriasiform Dermatitis MCR318 MCCPD
Microcephaly, Cortical Malformations, and Mental Retardation MCR098
Microcephaly, Epilepsy, and Diabetes Syndrome MCR209 MEDS
Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy MCR123 MCPHSBA
Microcephaly, Progressive, Seizures, and Cerebral and Cerebellar Atrophy MCR226 MSCCA
Microcephaly, Seizures, and Developmental Delay MCR064 MCSZ
Microcephaly, Short Stature, and Impaired Glucose Metabolism MCR235 MSSGM1
Microcephaly, Short Stature, and Impaired Glucose Metabolism 2 MCR316 MSSGM2
Microcoria, Congenital MCR067 MCOR
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus MCR220 MMCAT
Microcystic Adenoma MCR014
Microcystic Meningioma MCR001
Microcytic Anemia MCR018
Microglandular Adenosis MCR019
Micrognathia-Recurrent Infections-Behavioral Abnormalities-Mild Intellectual Disability Syndrome MCR319
Microhydranencephaly MCR025 MHAC
Microinvasive Cervical Squamous Cell Carcinoma MCR015
Microinvasive Gastric Cancer MCR011
Microlissencephaly MCR099
Microphthalmia MCR013
Microphthalmia with Coloboma 3 MCR136 MCOPCTI
Microphthalmia with Coloboma 5 MCR127 MCOPCB5
Microphthalmia with Coloboma 6, Digenic MCR110 MCOPCB6
Microphthalmia with Limb Anomalies MCR165 OAS
Microphthalmia, Isolated 1 MCR124 MCOP1
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 Coloboma 10 MCR271 MCOPCB10
Microphthalmia, Isolated, with Coloboma 7 MCR210 MCOPCB7
Microphthalmia, Isolated, with Coloboma 9 MCR214 MCOPCB9
Microphthalmia, Syndromic 1 MCR263 MCOPS1
Microphthalmia, Syndromic 11 MCR217 MCOPS11
Microphthalmia, Syndromic 12 MCR212 MCOPS12
Microphthalmia, Syndromic 13 MCR228 MCOPS13
Microphthalmia, Syndromic 14 MCR227 MCOPS14
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 MCOPCB8
Microscopic Colitis MCR191
Microscopic Polyangiitis MCR088 MPA
Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or Without Secondary Glaucoma MCR253 MSPKA
Microsporidiosis MCR020
Microtia MCR103
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma MCR242
Microtia, Hearing Impairment, and Cleft Palate MCR119 MCRT
Microvascular Complications of Diabetes 1 MCR129 MVCD1
Microvascular Complications of Diabetes 1, Susceptibility MCR276
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
Microvillus Inclusion Disease MCR094 DIAR2
Mid-Dermal Elastolysis MDD015
Middle Cerebral Artery Infarction MDD003
Middle Ear Adenoma MDD008
Middle Ear Carcinoma MDD009
Middle Ear Cholesterol Granuloma MDD006
Middle Ear Disease MDD010
Middle Ear Squamous Cell Carcinoma MDD007
Middle Lobe Syndrome MDD005
Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis MDF002 MFHIEN
Midline Interhemispheric Variant of Holoprosencephaly MDL020 MIH
Migraine with Aura MGR003
Migraine with Aura 7 MGR025
Migraine with Aura 9 MGR027
Migraine with Brainstem Aura MGR035 MBA
Migraine with or Without Aura 1 MGR028
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, Susceptibility 13 MGR034 MGR13
Migraine Without Aura 4 MGR023
Migraine, Familial Hemiplegic, 1 MGR032 FHM1
Migraine, Familial Hemiplegic, 2 MGR030 FHM2
Migraine, Familial Hemiplegic, 3 MGR031 FHM3
Migraine, Familial Typical 2 MGR029
Migraine, with or Without Aura 13 MGR019 MGR13
Mikulicz Disease MKL001
Mild Canavan Disease MLD009
Mild Hemophilia a MLD013
Mild Hemophilia B MLD014
Mild Hyperphenylalaninemia MLD011 MHPA
Mild Phenylketonuria MLD010 MPKU
Mild Phosphoribosylpyrophosphate Synthetase Superactivity MLD015
Mild Pre-Eclampsia MLD002
Miles-Carpenter Syndrome MLS013 MCS
Miles-Carpenter X-Linked Mental Retardation Syndrome MLS002 MCS
Miliaria MLR009
Miliaria Rubra MLR001
Miliary Tuberculosis MLR002
Milk Allergy MLK006
Milker's Nodule MLK001
Miller Fisher Syndrome MLL002
Miller Syndrome MLL012 POADS
Miller-Dieker Lissencephaly Syndrome MLL018 MDLS
Mineral Metabolism Disease MNR003
Minicore Myopathy with External Ophthalmoplegia MNC011 MMDO
Minimal Pigment Oculocutaneous Albinism Type 1 MNM005
Mirage Syndrome MRG013 MIRAGE
Mirror Movements 1 MRR011 MRMV1
Mirror Movements 2 MRR010 MRMV2
Mirror Movements 3 MRR012 MRMV3
Mismatch Repair Cancer Syndrome MSM014 MMRCS
Mitchell-Riley Syndrome MTC096 MTCHRS
Mite Infestation MTN002
Mitochondrial Cardiomyopathy MTC028
Mitochondrial Complex Deficiency, Nuclear Type 4 MTC092 MC5DN4
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 5 MTC099 MC3DN5
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 MTC021
Mitochondrial Complex V Deficiency, Mitochondrial 1 MTC080 MC5DM1
Mitochondrial Complex V Deficiency, Mitochondrial 2 MTC082 MC5DM2
Mitochondrial Disorders MTC069
Mitochondrial Dna Deletion Syndromes MTC014
Mitochondrial Dna Depletion Syndrome 1 MTC061 MTDPS1
Mitochondrial Dna Depletion Syndrome 11 MTC078 MTDPS11
Mitochondrial Dna Depletion Syndrome 12 MTC086 MTDPS12B
Mitochondrial Dna Depletion Syndrome 12a, Cardiomyopathic Type MTC124 MTDPS12A
Mitochondrial Dna Depletion Syndrome 13 MTC088 MTDPS13
Mitochondrial Dna Depletion Syndrome 14, Cardioencephalomyopathic Type MTC118 MTDPS14
Mitochondrial Dna Depletion Syndrome 15, Hepatocerebral Type MTC125 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 MTC033
Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form MTC034
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form MTC093
Mitochondrial Dna Depletion Syndrome, Mngie Form MTC084
Mitochondrial Dna Depletion Syndrome, Myopathic Form MTC035
Mitochondrial Dna-Associated Leigh Syndrome MTC112 MILS
Mitochondrial Dna-Associated Leigh Syndrome and Narp MTC015
Mitochondrial Encephalomyopathy MTC004
Mitochondrial Infantile Bilateral Striatal Necrosis MTC081 MIBSN
Mitochondrial Membrane Protein-Associated Neurodegeneration MTC036 MPAN
Mitochondrial Metabolism Disease MTC005
Mitochondrial Myopathy and Sideroblastic Anemia 1 MTC064 MLASA1
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
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 Recessive Ataxia Syndrome MTC057 SANDO
Mitochondrial Respiratory Chain Complex Ii Deficiency, Sdha-Related MTC042
Mitochondrial Respiratory Chain Complex Ii Deficiency, Sdhaf1-Related MTC041
Mitochondrial Respiratory Chain Complex Ii Deficiency, Sdhd-Related MTC117
Mitochondrial Respiratory Chain Complex Iii Deficiency, Bcs1l-Related MTC044
Mitochondrial Respiratory Chain Complex Iii Deficiency, Cyc1-Related MTC120
Mitochondrial Respiratory Chain Complex Iii Deficiency, Lyrm7-Related MTC121
Mitochondrial Respiratory Chain Complex Iii Deficiency, Ttc19-Related MTC045
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcc2-Related MTC122
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcc3-Related MTC123
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcrb-Related MTC046
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcrq Related MTC047
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcrq2 Related MTC110
Mitochondrial Respiratory Chain Complex Iii, Cytochrome B Subunit MTC048
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency MTC108 ECHS1D
Mitral Atresia MTR027
Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones MTR028 CSCF
Mitral Valve Disease MTR012
Mitral Valve Insufficiency MTR002
Mitral Valve Prolapse 2 MTR077 MVP2
Mitral Valve Prolapse, Myxomatous 2 MTR041 MVP2
Mitral Valve Prolapse, Myxomatous 3 MTR042
Mitral Valve Stenosis MTR003
Mixed Astrocytoma-Ependymoma MXD011
Mixed Cell Adenoma MXD020
Mixed Cell Type Cancer MXD023
Mixed Cerebral Palsy MXD001
Mixed Connective Tissue Disease MXD005 MCTD
Mixed Ductal-Endocrine Carcinoma MXD014
Mixed Endometrial Stromal and Smooth Muscle Tumor MXD017
Mixed Germ Cell Cancer MXD025
Mixed Germ Cell Tumor MXD032
Mixed Glioma MXD026
Mixed Gonadal Dysgenesis MXD016
Mixed Hepatoblastoma MXD007
Mixed Lacrimal Gland Cancer MXD003
Mixed Liposarcoma MXD006
Mixed Malaria MXD019
Mixed Oligodendroglioma-Astrocytoma MXD012
Mixed Type Thymoma MXD027
Miyoshi Muscular Dystrophy 1 MYS033 MMD1
Miyoshi Muscular Dystrophy 2 MYS019
Miyoshi Muscular Dystrophy 3 MYS014 MMD3
Mkks-Related Bardet-Biedl Syndrome MKK001 BBS6
Mks1-Related Bardet-Biedl Syndrome MKS001 BBS13
Mks1-Related Meckel Syndrome MKS002
Mlc1-Related Megalencephalic Leukoencephalopathy with Subcortical Cysts MLC001
Mlh1-Related Lynch Syndrome MLH002
Mlh1-Related Muir-Torre Syndrome MLH003
Mlh1-Related Turcot Syndrome MLH004
Mlh3-Related Lynch Syndrome MLH005
Mmaa-Related Methylmalonic Acidemia MMR001
Mmab-Related Methylmalonic Acidemia MMB004
Mmadhc-Related Methylmalonic Acidemia MMD001
Mn1 MN1001 MN1
Moderate and Severe Traumatic Brain Injury MDR006
Moderately Severe Hemophilia a MDR007
Moderately Severe Hemophilia B MDR008
Mody, Type I MDY005 MODY1
Mody, Type Ii MDY003 MODY2
Mody, Type Iii MDY004 MODY3
Mody, Type Iv MDY006 MODY4
Moebius Syndrome MBS002 MBS
Mohr-Tranebjaerg Syndrome MHR001 MTS
Molluscum Contagiosum MLL001
Molybdenum Cofactor Deficiency MLY001 MOCOD
Molybdenum Cofactor Deficiency a MLY006 MOCODA
Molybdenum Cofactor Deficiency B MLY005 MOCODB
Molybdenum Cofactor Deficiency C MLY007 MOCODC
Mondini Dysplasia MND005
Mongolian Spot MNG001
Monilethrix MNL001 MNLIX
Monkeypox MNK002
Monocarboxylate Transporter 1 Deficiency MNC019 MCT1D
Monoclonal Gammopathy of Uncertain Significance MNC006 MGUS
Monoclonal Paraproteinemia MNC004
Monocytic Leukemia MNC007
Monofixation Syndrome MNF001
Monogenic Diabetes MNG006
Monogenic Non-Syndromic Obesity, Autosomal Recessive MNG004
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
Monophasic Synovial Sarcoma MNP001
Monosomy 21 MNS008
Monosomy 22 MNS014
Monosomy 9q22.3 MNS011
Monostotic Fibrous Dysplasia MNS012
Mood Disorder MDD011
Mooren's Ulcer MRN002
Morbid Obesity MRB003
Morbid Obesity and Spermatogenic Failure MRB006 MOSPGF
Morgagni Cataract MRG001
Morpheaform Basal Cell Carcinoma MRP002
Morphine Dependence MRP001
Morvan's Fibrillary Chorea MRV001
Mosaic Trisomy 8 MSC020
Mosaic Variegated Aneuploidy Syndrome MSC022
Mosaic Variegated Aneuploidy Syndrome 1 MSC109 MVA1
Mosaic Variegated Aneuploidy Syndrome 2 MSC106 MVA2
Motion Sickness MTN003
Motor Neuron Disease MTR014
Motor Peripheral Neuropathy MTR007 HSMN
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 6 with Achalasia MYM008 MYMY6
Moyamoya Disease MYM002 MYMY
Moyamoya Disease 2 MYM004 MYMY2
Moyamoya Disease 3 MYM005
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism MYM012
Moyamoya Disease 5 MYM003 MYMY5
Mpph Syndrome MPP001 MPPH
Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome MPV001 NN
Mrpl40-Related Disorder MRP004
Ms4a1-Related Common Variable Immune Deficiency MS4001 CVID5
Msh2-Related Lynch Syndrome MSH002
Msh2-Related Muir-Torre Syndrome MSH003
Msh2-Related Turcot Syndrome MSH004
Msh6-Related Lynch Syndrome MSH005
Msh6-Related Turcot Syndrome MSH006
Msx2-Related Craniosynostosis MSX001 CRS2
Mt-Co1-Related Hearing Loss and Deafness MTC052
Mt-Cyb-Related Recurrent Myoglobinuria MTC053
Mt-Rnr1-Related Hearing Loss and Deafness MTR037
Mt-Ts1-Related Hearing Loss and Deafness MTT003
Mt-Tt Related Parkinson Disease Susceptibility MTT006
Mthfr Deficiency MTH027
Mthfr Gene Mutation MTH044
Mthfr Thermolabile Variant MTH028
Mthfr-Related Altered Drug Metabolism MTH063
Mu Chain Disease MCH003
Mucinoses MCN011
Mucinous Adenocarcinoma MCN001
Mucinous Adenocarcinoma of the Appendix MCN018
Mucinous Adenofibroma MCN006
Mucinous Cystadenocarcinoma MCN008
Mucinous Cystadenofibroma MCN010
Mucinous Intrahepatic Cholangiocarcinoma MCN005
Mucinous Ovarian Cystadenoma MCN003
Mucinous Stomach Adenocarcinoma MCN009
Mucinous Tubular and Spindle Renal Cell Carcinoma MCN004
Muckle-Wells Syndrome MCK007 MWS
Mucocele of Appendix MCC004
Mucocele of Salivary Gland MCC003
Mucociliary Clearance Disorder MCC011
Mucocutaneous Leishmaniasis MCC002
Mucoepidermoid Carcinoma MCP006 MEC
Mucoepidermoid Esophageal Carcinoma MCP008
Mucoepidermoid Thyroid Carcinoma MCP007
Mucolipidoses MCL022
Mucolipidosis Ii Alpha/beta MCL062 MLII
Mucolipidosis Iii Alpha/beta MCL046 MLIIIA
Mucolipidosis Iii Gamma MCL016 MLIIIC
Mucolipidosis Iv MCL013 ML4
Mucopolysaccharidisis Type Iiia MCP027 MPS3A
Mucopolysaccharidoses MCP033
Mucopolysaccharidosis MCP010 MPSPS
Mucopolysaccharidosis Ih MCP012 MPS1H
Mucopolysaccharidosis Ih/s MCP036 MPS1H/S
Mucopolysaccharidosis Ii MCP009 MPS2
Mucopolysaccharidosis Iii MCP001 MPS3
Mucopolysaccharidosis is MCP037 MPS1S
Mucopolysaccharidosis Iv MCP004 MPS4
Mucopolysaccharidosis Iva MCP038 MPS4A
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 Iiib MCP026 MPS3B
Mucopolysaccharidosis Type Iiic MCP020 MPS3C
Mucopolysaccharidosis Type Iiid MCP014 MPS3D
Mucopolysaccharidosis Type Ivb MCP023 MPS4B
Mucopolysaccharidosis Type Ix MCP015 MPS9
Mucopolysaccharidosis Type Vi MCP024 MPS6
Mucopolysaccharidosis Vii MCP003 MPS7
Mucosal Melanoma MCS004
Mucositis MCS002
Muenke Syndrome MNK003 MNKS
Muir-Torre Syndrome MRT001 MRTES
Mulibrey Nanism MLB001 MUL
Mullerian Aplasia MLL009
Mullerian Aplasia and Hyperandrogenism MLL011 MULLAPL
Multicentric Carpotarsal Osteolysis Syndrome MLT092 MCTO
Multicentric Castleman Disease MLT113 MCD
Multicentric Osteolysis Nephropathy MLT033
Multicentric Osteolysis of Torg MLT064
Multicentric Osteolysis, Nodulosis, and Arthropathy MLT065 MONA
Multicentric Papillary Thyroid Carcinoma MLT005
Multicentric Reticulohistiocytosis MLT016
Multicystic Dysplastic Kidney MLT084 MCDK
Multidrug-Resistant Tuberculosis MLT006
Multifocal Choroiditis MLT035
Multifocal Dystonia MLT132
Multifocal Motor Neuropathy MLT075 MMN
Multifocal Osteogenic Sarcoma MLT017
Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus MLT117
Multilocular Clear Cell Renal Cell Carcinoma MLT003
Multiminicore Disease MLT028 MMD
Multinodular Goiter MLT008
Multiple Acyl-Coa Dehydrogenation Deficiency, Mild Type MLT129
Multiple Acyl-Coa Dehydrogenation Deficiency, Severe Neonatal Type MLT130
Multiple Benign Circumferential Skin Creases on Limbs MLT104 CCSF
Multiple Carboxylase Deficiency MLT018 MCD
Multiple Chemical Sensitivity MLT001
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 Cutaneous and Uterine Leiomyomas MLT066 MCUL
Multiple Enchondromatosis, Maffucci Type MLT145
Multiple Endocrine Neoplasia MLT074 MEA
Multiple Endocrine Neoplasia 1 MLT136 MEN1
Multiple Endocrine Neoplasia Iia MLT024 MEN2A
Multiple Endocrine Neoplasia Iib MLT025 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, Dominant MLT030
Multiple Epiphyseal Dysplasia, Recessive MLT031 EDM4
Multiple Familial Trichoepithelioma MLT048 EAC
Multiple Fibroadenomas of the Breast MLT120 MFAB
Multiple Joint Dislocations, Short Stature, Craniofacial Dysmorphism, and Congenital Heart Defects MLT123 JDSCD
Multiple Mitochondrial Dysfunctions Syndrome MLT027 MMDS
Multiple Mitochondrial Dysfunctions Syndrome 1 MLT068 MMDS1
Multiple Mitochondrial Dysfunctions Syndrome 2 MLT069 MMDS2
Multiple Mitochondrial Dysfunctions Syndrome 3 MLT119 MMDS3
Multiple Mitochondrial Dysfunctions Syndrome 4 MLT139 MMDS4
Multiple Mucosal Neuroma MLT011
Multiple Myeloma MLT019 MM
Multiple Paragangliomas Associated with Polycythemia MLT106
Multiple Personality Disorder MLT010
Multiple Pterygium Syndrome, Lethal Type MLT134 LMPS
Multiple Sclerosis 2 MLT093
Multiple Sclerosis 3 MLT094 MS3
Multiple Sclerosis 4 MLT095
Multiple Sclerosis 5 MLT124 MS5
Multiple Sclerosis, Disease Progression, Modifier of MLT077 MS
Multiple Self-Healing Squamous Epithelioma, Susceptiblity to MLT122 MSSE
Multiple Sulfatase Deficiency MLT135 MSD
Multiple Symmetrical Lipomatosis MLT002
Multiple Synostoses Syndrome MLT072
Multiple Synostoses Syndrome 1 MLT059 SYNS1
Multiple Synostoses Syndrome 2 MLT060 SYNS2
Multiple Synostoses Syndrome 3 MLT078 SYNS3
Multiple System Atrophy MLT021 MSA1
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 Disorders MSC033
Muscle Eye Brain Disease MSC077 MEB
Muscle Glycogenosis MSC006 GSD9D
Muscle Hypertrophy MSC007 MSLHP
Muscle Strength Quantitative Trait Locus 1 MSC054
Muscle Tissue Disease MSC004
Muscular Atrophy MSC003
Muscular Dystrophy MSC005
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, 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, 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, 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, 9 MSC100 MDDGC9
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies, Type a, 11 MSC094 MDDGA11
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies, Type a, 8 MSC096 MDDGA8
Muscular Dystrophy, Congenital MSC124 MDCL
Muscular Dystrophy, Congenital Merosin-Deficient MSC039 MDC1A
Muscular Dystrophy, Congenital, 1b MSC050
Muscular Dystrophy, Congenital, Due to Itga7 Deficiency MSC052 MDCI
Muscular Dystrophy, Congenital, Megaconial Type MSC028 MDCMC
Muscular Dystrophy, Congenital, Merosin-Positive MSC029
Muscular Dystrophy, Limb-Girdle, Type 1a MSC115 LGMD1A
Muscular Dystrophy, Limb-Girdle, Type 1b MSC112 LGMD1B
Muscular Dystrophy, Limb-Girdle, Type 1e MSC117 LGMD1E
Muscular Dystrophy, Limb-Girdle, Type 1f MSC057 LGMD1F
Muscular Dystrophy, Limb-Girdle, Type 1h MSC058
Muscular Dystrophy, Limb-Girdle, Type 2a MSC121 LGMD2A
Muscular Dystrophy, Limb-Girdle, Type 2b MSC113 LGMD2B
Muscular Dystrophy, Limb-Girdle, Type 2c MSC120 LGMD2C
Muscular Dystrophy, Limb-Girdle, Type 2d MSC123 LGMD2D
Muscular Dystrophy, Limb-Girdle, Type 2e MSC114 LGMD2E
Muscular Dystrophy, Limb-Girdle, Type 2f MSC116 LGMD2F
Muscular Dystrophy, Limb-Girdle, Type 2g MSC122 LGMD2G
Muscular Dystrophy, Limb-Girdle, Type 2h MSC119 LGMD2H
Muscular Dystrophy, Limb-Girdle, Type 2j MSC063 LGMD2J
Muscular Dystrophy, Limb-Girdle, Type 2l MSC059 LGMD2L
Muscular Dystrophy, Limb-Girdle, Type 2q MSC062 LGMD2Q
Muscular Dystrophy, Limb-Girdle, Type 2r MSC095 LGMD2R
Muscular Dystrophy, Limb-Girdle, Type Ic MSC049 LGMD1C
Muscular Dystrophy, Rigid Spine, 1 MSC051 RSMD1
Muscular Phosphorylase Kinase Deficiency MSC031
Musculocontractural Ehlers-Danlos Syndrome MSC134 ATCS
Musk-Related Congenital Myasthenic Syndrome MSK001
Mut-Related Methylmalonic Acidemia MTR038
Mutagen Sensitivity MTG002
Mutism MTS001
Mutyh-Associated Polyposis MTY001
Myasthenia Gravis MYS003 MG
Myasthenia Gravis Congenital MYS011
Myasthenia Gravis with Thymus Hyperplasia MYS007
Myasthenia, Congenital, 12, with Tubular Aggregates MYS045 CMS12
Myasthenia, Limb-Girdle, with Tubular Aggregates MYS015
Myasthenic Syndrome, Congenital, 10 MYS052 CMS10
Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency MYS057 CMS11
Myasthenic Syndrome, Congenital, 13, with Tubular Aggregates MYS058 CMS13
Myasthenic Syndrome, Congenital, 14, with Tubular Aggregates MYS053 CMS14
Myasthenic Syndrome, Congenital, 15, Without Tubular Aggregates MYS043 CMS15
Myasthenic Syndrome, Congenital, 16 MYS064 CMS16
Myasthenic Syndrome, Congenital, 17 MYS056 CMS17
Myasthenic Syndrome, Congenital, 18 MYS065 CMS18
Myasthenic Syndrome, Congenital, 1a, Slow-Channel MYS046 CMS1A
Myasthenic Syndrome, Congenital, 1b, Fast-Channel MYS047 CMS1B
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, with Pre- and Postsynaptic Defects MYS042 CMS8
Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency MYS054 CMS9
Mybpc3-Related Dilated Cardiomyopathy MYB002
Mybpc3-Related Familial Hypertrophic Cardiomyopathy MYB003
Mycetoma MYC012
Mycobacterium Abscessus MYC013
Mycobacterium Avium Complex Disease MYC002 MAI
Mycobacterium Chelonae MYC014
Mycobacterium Fortuitum MYC015
Mycobacterium Gordonae MYC016
Mycobacterium Kansasii MYC017
Mycobacterium Malmoense MYC018
Mycobacterium Marinum MYC019
Mycobacterium Tuberculosis 2 MYC054
Mycobacterium Tuberculosis 3 MYC055
Mycobacterium Tuberculosis, Susceptibility to Infection by MYC020
Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included MYC073
Mycoplasmal Pneumonia MYC022
Mycosis Fungoides MYC006 MF
Myd88 Deficiency MYD002 MYD88D
Myelitis MYL001
Myelocerebellar Disorder MYL017 ATXPC
Myelocystocele MYL044
Myelodysplasia and Leukemia Syndrome with Monosomy 7 MYL048
Myelodysplastic Myeloproliferative Cancer MYL004
Myelodysplastic Syndrome MYL009 MDS
Myelodysplastic Syndrome, Susceptibility, Gata2-Related MYL039
Myelofibrosis MYL005
Myelofibrosis with Myeloid Metaplasia, Somatic MYL045 MYELOF
Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities MYL054 SCLL
Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 MYL059
Myeloid Leukemia MYL006
Myeloid Neoplasm Associated with Pdgfra Rearrangement MYL043
Myeloid Neoplasm Associated with Pdgfrb Rearrangement MYL042
Myeloid Neoplasms Associated with Pdgfrb Rearrangement MYL061
Myeloid Sarcoma MYL003
Myeloid/lymphoid or Mixed Lineage Leukemia MYL055 MLL
Myelomeningocele MYL020
Myelopathy, Htlv-1-Associated MYL057 TSP
Myeloperoxidase Deficiency MYL013 MPOD
Myelophthisic Anemia MYL002
Myeloproliferative Disorder with Eosinophilia MYL015 MPE
Myeloproliferative Neoplasm MYL031 CMPD
Myeloproliferative Neoplasms, Familial MYL052
Myeloproliferative Syndrome, Transient MYL058 MST
Myh-9 Related Disease MYH015
Myh11-Related Thoracic Aortic Aneurysms and Aortic Dissections MYH005 AAT4
Myh3-Related Arthrogryposis Multiplex Congenita, Distal, Type 2b MYH006
Myh6-Related Dilated Cardiomyopathy MYH007
Myh6-Related Familial Hypertrophic Cardiomyopathy MYH008
Myh7-Related Congenital Fiber-Type Disproportion MYH013
Myh7-Related Dilated Cardiomyopathy MYH009
Myh7-Related Familial Hypertrophic Cardiomyopathy MYH010
Myh7-Related Myosin Storage Myopathy MYH011
Myh9 Related Thrombocytopenia MYH004
Myhre Syndrome MYH012 MYHRS
Myiasis MYS004
Myl2-Related Familial Hypertrophic Cardiomyopathy MYL021
Myl3-Related Familial Hypertrophic Cardiomyopathy MYL022
Myl4-Related Familial Atrial Fibrillation MYL063 ATFB18
Mylk-Related Thoracic Aortic Aneurysms and Aortic Dissections MYL023 AAT7
Myoblastoma MYB001
Myocardial Infarction MYC007 MCI1
Myocardial Infarction 2 MYC058
Myocardial Infarction, Susceptibility to, 1 MYC029
Myocardial Stunning MYC005
Myocarditis MYC008
Myoclonic Astatic Epilepsy MYC023
Myoclonic Cerebellar Dyssynergia MYC001
Myoclonic Epilepsy Associated with Ragged-Red Fibers MYC072 MERRF
Myoclonic Epilepsy Myopathy Sensory Ataxia MYC030 SCAE
Myoclonic Epilepsy of Infancy MYC068
Myoclonic Epilepsy, Infantile, Familial MYC048 FIME
Myoclonic Epilepsy, Juvenile 1 MYC070 EJM1
Myoclonic-Astastic Epilepsy MYC069 MAE
Myoclonic-Atonic Epilepsy MYC071 MAE
Myoclonus MYC033
Myoclonus Epilepsy MYC026
Myoclonus, Familial Cortical MYC066 FCM
Myoepithelial Carcinoma MYP002
Myofascial Pain Syndrome MYF002
Myofibrillar Myopathy MYF003
Myofibrillar Myopathy 7 MYF009 MFM7
Myofibroma MYF001
Myofibromatosis, Infantile 2 MYF008 IMF2
Myofibromatosis, Infantile, 1 MYF007 IMF1
Myoglobinuria MYG005
Myoglobinuria Recurrent MYG003
Myoglobinuria, Acute Recurrent, Autosomal Recessive MYG004 ARARM
Myokymia 1 with or Without Hypomagnesemia MYK003
Myoma MYM001 MYOMA
Myopathic Intestinal Pseudoobstruction MYP066
Myopathy MYP004
Myopathy Due to Cpt Ii Deficiency MYP007 CPT2D
Myopathy Due to Myoadenylate Deaminase Deficiency MYP071 MMDD
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 Lactic Acidosis, Hereditary MYP097 MEIS
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset MYP093 EMARDD
Myopathy, Centronuclear MYP101 CNM1
Myopathy, Centronuclear, 3 MYP096 CNM3
Myopathy, Centronuclear, 4 MYP098 CNM4
Myopathy, Centronuclear, Autosomal Recessive MYP102 CNM2
Myopathy, Congenital, Compton-North MYP038 MYPCN
Myopathy, Congenital, with Fiber-Type Disproportion MYP091 CFTD
Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked MYP039
Myopathy, Distal, 3 MYP112 MPD3
Myopathy, Distal, 4 MYP095 MPD4
Myopathy, Distal, 5 MYP116 MPD5
Myopathy, Distal, Tateyama Type MYP067 MPDT
Myopathy, Distal, with Anterior Tibial Onset MYP035 DMAT
Myopathy, Early-Onset, with Fatal Cardiomyopathy MYP092 EOMFC
Myopathy, Isolated Mitochondrial, Autosomal Dominant MYP099 IMMD
Myopathy, Lactic Acidosis, and Sideroblastic Anemia MYP108
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, 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, 8 MYP118 MFM8
Myopathy, Myofibrillar, Fatal Infantile Hypertrophy, Alpha-B Crystallin-Related MYP083 MFMFIH-CRYAB
Myopathy, Myosin Storage, Autosomal Dominant MYP105 MSMA
Myopathy, Myosin Storage, Autosomal Recessive MYP106 MSMB
Myopathy, Proximal, with Early Respiratory Muscle Involvement MYP103 HMERF
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
Myopericytoma MYP064
Myopia MYP006
Myopia 10 MYP044
Myopia 14 MYP069
Myopia 20, Autosomal Dominant MYP084
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 6 MYP018 MYP6
Myopia 7 MYP040
Myopia 8 MYP041
Myopia 9 MYP048
Myopia, High, with Cataract and Vitreoretinal Degeneration MYP073 MCVD
Myopia, X-Linked MYP024
Myosclerosis, Congenital MYS021 MYOSAR
Myosin Storage Myopathy MYS032
Myositis MYS005
Myositis Fibrosa MYS002
Myositis Ossificans MYS001
Myostatin-Related Muscle Hypertrophy MYS010 MSLHP
Myotonia MYT011
Myotonia Congenita MYT023
Myotonia Congenita, Atypical, Acetazolamide-Responsive MYT015 MYOSCN4A
Myotonia Congenita, Dominant MYT013 MCAD
Myotonia Congenita, Recessive MYT012 MCAR
Myotonic Disease MYT003
Myotonic Dystrophy MYT002
Myotonic Dystrophy 1 MYT021 DM1
Myotonic Dystrophy 2 MYT020 DM2
Myotubular Myopathy with Abnormal Genital Development MYT025
Myotubular Myopathy, X-Linked MYT022 CNMX
Myoz2-Related Familial Hypertrophic Cardiomyopathy MYZ001
Mypn-Related Cardiomyopathy MYP109
Mypn-Related Familial Restrictive Cardiomyopathy MYP115 RCM4
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
Myxopapillary Ependymoma MYX001
Myxosarcoma MYX007