Disease Name Symbol Acronym
Machado-Joseph Disease MCH002 MJD
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 MACID
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation MCR321 MDFPMR
Macrocephaly/autism Syndrome MCR096 MCEPHAS
Macrocephaly/megalencephaly Syndrome, Autosomal Recessive MCR237 MGCPH
Macrocytic Anemia MCR017
Macrodactyly MCR364 MADAC
Macrodactyly of Fingers, Unilateral MCR188
Macrodactyly of Toes MCR185
Macrodactyly of Toes, Unilateral MCR190
Macroglobulinemia MCR004
Macroglobulinemia, Waldenstrom 1 MCR161 WM1
Macroglobulinemia, Waldenstrom 2 MCR162 WM2
Macroglossia MCR037
Macrophage Activation Syndrome MCR225
Macrophthalmia, Colobomatous, with Microcornea MCR317 MACOM
Macrostomia, Isolated MCR302
Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss MCR359 MATINS
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related MCR125 MAD-TUBB1
Macrozoospermia MCR265 SPGF5
Macs Syndrome MCS006 MACS
Macular Amyloidosis MCL047
Macular Degeneration, Age-Related, 1 MCL042 ARMD1
Macular Degeneration, Age-Related, 10 MCL030 ARMD10
Macular Degeneration, Age-Related, 11 MCL032 ARMD11
Macular Degeneration, Age-Related, 12 MCL051 ARMD12
Macular Degeneration, Age-Related, 13 MCL052 ARMD13
Macular Degeneration, Age-Related, 14 MCL078 ARMD14
Macular Degeneration, Age-Related, 15 MCL065 ARMD15
Macular Degeneration, Age-Related, 2 MCL043 ARMD2
Macular Degeneration, Age-Related, 4 MCL038 ARMD4
Macular Degeneration, Age-Related, 5 MCL077 ARMD5
Macular Degeneration, Age-Related, 6 MCL036 ARMD6
Macular Degeneration, Age-Related, 7 MCL041 ARMD7
Macular Degeneration, Age-Related, 8 MCL039 ARMD8
Macular Degeneration, Age-Related, 9 MCL044 ARMD9
Macular Degeneration, Early-Onset MCL058 EOMD
Macular Degeneration, X-Linked Atrophic MCL029 MDXLA
Macular Dystrophy with Central Cone Involvement MCL057 CCMD
Macular Dystrophy, Concentric Annular MCL018 BCAMD
Macular Dystrophy, Corneal MCL075 MCD
Macular Dystrophy, Dominant Cystoid MCL027 DCMD
Macular Dystrophy, Patterned, 1 MCL059 MDPT1
Macular Dystrophy, Patterned, 2 MCL071 MDPT2
Macular Dystrophy, Patterned, 3 MCL070 MDPT3
Macular Dystrophy, Retinal, 1, North Carolina Type MCL069 MCDR1
Macular Dystrophy, Retinal, 2 MCL035 MCDR2
Macular Dystrophy, Retinal, 3 MCL026 MCDR3
Macular Dystrophy, Vitelliform, 1 MCL073 VMD1
Macular Dystrophy, Vitelliform, 2 MCL066 VMD2
Macular Dystrophy, Vitelliform, 3 MCL060 VMD3
Macular Dystrophy, Vitelliform, 4 MCL061 VMD4
Macular Dystrophy, Vitelliform, 5 MCL056 VMD5
Macular Holes MCL003
Macular Retinal Edema MCL006
Macular Telangiectasia Type 2 MCL079 IJT
Madelung Deformity MDL024
Madras Motor Neuron Disease MDR004 MMND
Majeed Syndrome MJD001 MJDS
Major Affective Disorder 1 MJR007 MAFD1
Major Affective Disorder 2 MJR008 MAFD2
Major Affective Disorder 3 MJR021 MAFD3
Major Affective Disorder 4 MJR004 MAFD4
Major Affective Disorder 5 MJR006 MAFD5
Major Affective Disorder 6 MJR003 MAFD6
Major Affective Disorder 7 MJR023 MAFD7
Major Affective Disorder 8 MJR022 MAFD8
Major Affective Disorder 9 MJR024 MAFD9
Major Depressive Disorder MJR001 MDD
Major Depressive Disorder 1 MJR013 MDD1
Major Depressive Disorder 2 MJR014 MDD2
Mal De Meleda MLD006 MDM
Malaria MLR004 CM
Malaria, Mild MLR020 MAL
Male Infertility MLN007
Male Infertility Due to Acephalic Spermatozoa MLN078
Male Infertility Due to Obstructive Azoospermia MLN085
Male Infertility Due to Sperm Motility Disorder MLN081
Male Infertility with Azoospermia or Oligozoospermia Due to Single Gene Mutation MLN084
Male Infertility with Teratozoospermia Due to Single Gene Mutation MLN056
Male Reproductive Organ Benign Neoplasm MLR005
Male Reproductive Organ Cancer MLR006
Male Reproductive System Disease MLR007
Maleylacetoacetate Isomerase Deficiency MLY011 MAAID
Malformation Syndrome with Short Stature MLF005
Maligant Granulosa Cell Tumor of the Ovary MLG155
Malignant Acrospiroma MLG048
Malignant Anus Melanoma MLG038
Malignant Atrophic Papulosis MLG141
Malignant Biphasic Mesothelioma MLG011
Malignant Childhood Germ Cell Neoplasm MLG037
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 Epithelioid Hemangioendothelioma MLG145
Malignant Essential Hypertension MLG039
Malignant Fibrous Histiocytoma of Bone MLG014
Malignant Fibroxanthoma MLG065 MFH
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 Hemangioma MLG144
Malignant Histiocytosis MLG054
Malignant Hypertension MLG069
Malignant Hypertensive Renal Disease MLG004
Malignant Hyperthermia MLG056 MH
Malignant Hyperthermia 1 MLG147 MHS1
Malignant Hyperthermia 2 MLG148 MHS2
Malignant Hyperthermia 3 MLG149 MHS3
Malignant Hyperthermia 4 MLG150 MHS4
Malignant Hyperthermia 5 MLG151 MHS5
Malignant Hyperthermia 6 MLG152 MHS6
Malignant Hyperthermia of Anesthesia MLG143
Malignant Hyperthermia Susceptibility MLG086
Malignant Iris Melanoma MLG070
Malignant Leptomeningeal Tumor MLG071
Malignant Leydig Cell Tumor MLG072
Malignant Mesenchymoma MLG074
Malignant Migrating Partial Seizures of Infancy MLG120 MPEI
Malignant Otitis Externa MLG042
Malignant Ovarian Cyst MLG033
Malignant Ovarian Surface Epithelial-Stromal Neoplasm MLG076
Malignant Peripheral Nerve Sheath Tumor MLG077 MPNST
Malignant Peritoneal Mesothelioma MLG002
Malignant Pheochromocytoma MLG157
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 of the Ovary MLG154
Malignant Skin Fibrous Histiocytoma MLG007
Malignant Spindle Cell Melanoma MLG005
Malignant Spiradenoma MLG036 MES
Malignant Struma Ovarii MLG059
Malignant Syringoma MLG049
Malignant Teratoma MLG081
Malignant Triton Tumor MLG041 MTT
Malonyl-Coa Decarboxylase Deficiency MLN011 MLYCD DEFICIENCY
Mammary Paget's Disease MMM001
Mammary-Digital-Nail Syndrome MMM002 MDNS
Mammographic Density MMM006
Man1b1-Cdg MN1002
Mandibular Cancer MND001
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome MND021 MDPL
Mandibuloacral Dysplasia with Type a Lipodystrophy MND003 MADA
Mandibuloacral Dysplasia with Type B Lipodystrophy MND002 MADB
Mandibulofacial Dysostosis with Alopecia MND025 MFDA
Mandibulofacial Dysostosis with Mental Retardation MND028
Mandibulofacial Dysostosis, Guion-Almeida Type MND020 MFDGA
Manitoba Oculotrichoanal Syndrome MNT006 MOTA
Mannose-Binding Lectin Deficiency MNN034 MBLD
Mannosidosis, Alpha B, Lysosomal MNN047 MANSA
Mannosidosis, Beta a, Lysosomal MNN019 MANSB
Mansonelliasis MNS001
Mantle Cell Lymphoma MNT001 LCM
Maple Syrup Urine Disease MPL001 MSUD
Maple Syrup Urine Disease, Mild Variant MPL011 MSUDMV
Marantic Endocarditis MRN001
Marasmus MRS001
Marburg Hemorrhagic Fever MRB001 MHF
Marcus Gunn Phenomenon MRC002
Marden Walker Like Syndrome MRD001 VDEGS
Marden-Walker Syndrome MRD002 MWKS
Marek Disease MRK002
Marfan Syndrome MRF001 MFS
Marfanoid-Progeroid-Lipodystrophy Syndrome MRF021 MFLS
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
Marsili Syndrome MRS009 MARSIS
Martsolf Syndrome MRT007 MARTS
Masa Syndrome MSS001 MASA
Masp2 Deficiency MSP001 MASPD
Mast Cell Activation Syndrome MST020 MCAS
Mast Cell Neoplasm MST004
Mast Syndrome MST006 SPG21
Mast-Cell Leukemia MST002
Mast-Cell Sarcoma MST001
Masters-Allen Syndrome MST003
Mastitis MST005
Mastocytosis MST009
Mastocytosis, Cutaneous MST024 MASTC
Mastoiditis MST019
Maternal Uniparental Disomy MTR087
Maternal Uniparental Disomy of Chromosome 1 MTR051
Maternal Uniparental Disomy of Chromosome 16 MTR067
Maternal Uniparental Disomy of Chromosome 22 MTR064
Maternal Uniparental Disomy of Chromosome 4 MTR062
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, Type 1 MTR018 MODY1
Maturity-Onset Diabetes of the Young, Type 10 MTR044 MODY10
Maturity-Onset Diabetes of the Young, Type 11 MTR039 MODY11
Maturity-Onset Diabetes of the Young, Type 13 MTR075 MODY13
Maturity-Onset Diabetes of the Young, Type 14 MTR074 MODY14
Maturity-Onset Diabetes of the Young, Type 2 MTR019 MODY2
Maturity-Onset Diabetes of the Young, Type 3 MTR020 MODY3
Maturity-Onset Diabetes of the Young, Type 4 MTR021 MODY4
Maturity-Onset Diabetes of the Young, Type 6 MTR023 MODY6
Maturity-Onset Diabetes of the Young, Type 7 MTR024 MODY7
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction MTR082 MODY8
Maturity-Onset Diabetes of the Young, Type 9 MTR026 MODY9
Maxillary Cancer MXL017
Maxillary Sinus Adenoid Cystic Carcinoma MXL002
Maxillary Sinus Cancer MXL008
Maxillary Sinus Squamous Cell Carcinoma MXL004
Maxillary Sinusitis MXL015
Maxillonasal Dysplasia, Binder Type MXL016
Mayer-Rokitansky-Kuster-Hauser Syndrome MYR002 RKH SYNDROME
May-Thurner Syndrome MYT019
Mazabraud Syndrome MZB001
Mbd5 Haploinsufficiency MBD001 MAND
Mccune-Albright Syndrome MCC012 MAS
Mckusick-Kaufman Syndrome MCK005 MKKS
Mcleod Syndrome MCL009 MCLDS
Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency MCT002
Mda5 Deficiency MD5001
Meacham Syndrome MCH011 MEACHS
Mean Platelet Volume/count Quantitative Trait Locus 1 MNP022 MPVCQTL1
Mean Platelet Volume/count Quantitative Trait Locus 2 MNP023 MPVCQTL2
Mean Platelet Volume/count Quantitative Trait Locus 3 MNP024 MPVCQTL3
Mean Platelet Volume/count Quantitative Trait Locus 4 MNP025 MPVCQTL4
Mean Platelet Volume/count Quantitative Trait Locus 5 MNP026 MPVCQTL5
Mean Platelet Volume/count Quantitative Trait Locus 6 MNP027 MPVCQTL6
Measles MSL001
Mechanical Ectropion MCH001
Meckel Diverticulum MCK029
Meckel Syndrome 12 MCK026 MKS12
Meckel Syndrome 13 MCK028 MKS13
Meckel Syndrome, Type 1 MCK013 MKS1
Meckel Syndrome, Type 10 MCK035 MKS10
Meckel Syndrome, Type 11 MCK020 MKS11
Meckel Syndrome, Type 2 MCK031 MKS2
Meckel Syndrome, Type 3 MCK032 MKS3
Meckel Syndrome, Type 4 MCK033 MKS4
Meckel Syndrome, Type 5 MCK014 MKS5
Meckel Syndrome, Type 6 MCK012 MKS6
Meckel Syndrome, Type 7 MCK030 MKS7
Meckel Syndrome, Type 8 MCK034 MKS8
Meckel Syndrome, Type 9 MCK036 MKS9
Meconium Aspiration Syndrome MCN007 MAS
Meconium Ileus MCN017 MECIL
Mecr-Related Neurologic Disorder MCR373 DYT29
Med12-Related Disorders MD1001
Med13l Haploinsufficiency Syndrome MD1003 ASRAS
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
Mediastinal Neurilemmoma MDS020
Mediastinitis MDS022
Mediastinum Liposarcoma MDS002
Mediastinum Sarcoma MDS023
Mediastinum Teratoma MDS011
Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency MDM001 MCADD
Medullary Cystic Kidney Disease 1 MDL008 MCKD1
Medullary Cystic Kidney Disease 2 MDL021 MCKD2
Medullary Sponge Kidney MDL009 MSK
Medulloblastoma MDL005 MDB
Medulloepithelioma MDL002
Medullomyoblastoma MDL003
Meester-Loeys Syndrome MST021 MRLS
Megacolon MGC001
Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations MGC007 MCCCHCM
Megaesophagus MGS001
Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) MGK005
Megakaryocytic Leukemia MGK001 AMKL
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 MGL009 MLC1
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a MGL010 MLC2A
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b, Remitting, with or Without Mental Retardation MGL011 MLC2B
Megalencephaly MGL013
Megalencephaly, Autosomal Dominant MGL035
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome MGL038 MCAP
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 MGL030 MPPH1
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 MGL028 MPPH2
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 MGL029 MPPH3
Megaloblastic Anemia MGL001 IGS
Megaloblastic Anemia 1 MGL018 RH-MGA1
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency MGL012 DHFRD
Megalocornea MGL003
Mehmo Syndrome MHM001 MEHMO
Meibomian Cyst MBM001
Meier-Gorlin Syndrome 1 MRG008 MGORS1
Meier-Gorlin Syndrome 2 MRG009 MGORS2
Meier-Gorlin Syndrome 3 MRG010 MGORS3
Meier-Gorlin Syndrome 4 MRG011 MGORS4
Meier-Gorlin Syndrome 5 MRG012 MGORS5
Meier-Gorlin Syndrome 6 MRG014 MGORS6
Meier-Gorlin Syndrome 7 MRG015 MGORS7
Meier-Gorlin Syndrome 8 MRG016 MGORS8
Melancholia MLN003
Melanoacanthoma MLN005
Melanocytic Nevus Syndrome, Congenital MLN065 CMNS
Melanoma MLN008
Melanoma in Congenital Melanocytic Nevus MLN079
Melanoma of Soft Tissue MLN064
Melanoma, Cutaneous Malignant 1 MLN066 CMM1
Melanoma, Cutaneous Malignant 10 MLN055 CMM10
Melanoma, Cutaneous Malignant 2 MLN067 CMM2
Melanoma, Cutaneous Malignant 3 MLN075 CMM3
Melanoma, Cutaneous Malignant 4 MLN074 CMM4
Melanoma, Cutaneous Malignant 5 MLN076 CMM5
Melanoma, Cutaneous Malignant 6 MLN042 CMM6
Melanoma, Cutaneous Malignant 7 MLN040 CMM7
Melanoma, Cutaneous Malignant 8 MLN043 CMM8
Melanoma, Cutaneous Malignant 9 MLN077 CMM9
Melanoma, Uveal MLN069
Melanoma, Uveal 1 MLN039 UVM1
Melanoma, Uveal 2 MLN041 UVM2
Melanoma-Associated Retinopathy MLN046
Melanoma-Astrocytoma Syndrome MLN070 MASTS
Melanoma-Pancreatic Cancer Syndrome MLN047 FAMMMPC
Melanomatosis MLN002
Melanosis, Neurocutaneous MLN073 NCMS
Melanotic Medulloblastoma MLN004
Melanotic Neurilemmoma MLN009
Melanotic Neuroectodermal Tumor MLN001
Melioidosis MLD001
Melkersson-Rosenthal Syndrome MLK003 MRS
Melnick-Needles Syndrome MLN014 MNS
Melon Allergy MLN063
Melorheostosis MLR003
Melorheostosis with Osteopoikilosis MLR010
Membranoproliferative Glomerulonephritis MMB001 MPGN
Membranous Nephropathy MMB011 MBNP
Memory Quantitative Trait Locus MMR005 MEMRYQTL
Menarche, Age at, Quantitative Trait Locus 1 MNR013 MENAQ1
Menarche, Age at, Quantitative Trait Locus 2 MNR014 MENAQ2
Menarche, Age at, Quantitative Trait Locus 3 MNR015 MENAQ3
Mend Syndrome MND023 MEND
Meniere Disease MNR012
Meningeal Melanocytoma MNN001
Meningeal Melanoma MNN010
Meningeal Melanomatosis MNN008
Meninges Hemangiopericytoma MNN006
Meninges Sarcoma MNN011
Meningioma, Familial MNN043 MNGMA
Meningioma, Radiation-Induced MNN042 MNRI
Meningitis MNN013
Meningitis and Encephalitis MNN024
Meningocele MNN007
Meningococcal Infection MNN020
Meningococcal Meningitis MNN032
Meningococcemia MNN021
Meningoencephalitis MNN009
Meningoencephalocele MNN022
Meningothelial Meningioma MNN004
Meningovascular Neurosyphilis MNN005
Menke-Hennekam Syndrome 1 MNK005 MKHK1
Menke-Hennekam Syndrome 2 MNK006 MKHK2
Menkes Disease MNK001 MNKD
Menopause, Natural, Age at, Quantitative Trait Locus 1 MNP013 MENOQ1
Menopause, Natural, Age at, Quantitative Trait Locus 2 MNP017 MENOQ2
Menopause, Natural, Age at, Quantitative Trait Locus 4 MNP018 MENOQ4
Mental Depression MNT002
Mental Health Wellness 1 MNT312 MHW1
Mental Health Wellness 2 MNT313 MHW2
Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects MNT266 MRFACD
Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia MNT046 MICPCH
Mental Retardation with Language Impairment and with or Without Autistic Features MNT237 MRLIAF
Mental Retardation with Optic Atrophy, Deafness, and Seizures MNT308 GUST
Mental Retardation, Anterior Maxillary Protrusion, and Strabismus MNT118 MRAMS
Mental Retardation, Autosomal Dominant 10 MNT186 MRD10
Mental Retardation, Autosomal Dominant 11 MNT184 MRD11
Mental Retardation, Autosomal Dominant 13 MNT143 MRD13
Mental Retardation, Autosomal Dominant 18 MNT157 MRD18
Mental Retardation, Autosomal Dominant 20 MNT319 MRD20
Mental Retardation, Autosomal Dominant 21 MNT179 MRD21
Mental Retardation, Autosomal Dominant 22 MNT158 MRD22
Mental Retardation, Autosomal Dominant 23 MNT211 MRD23
Mental Retardation, Autosomal Dominant 24 MNT214 MRD24
Mental Retardation, Autosomal Dominant 26 MNT212 MRD26
Mental Retardation, Autosomal Dominant 29 MNT222 MRD29
Mental Retardation, Autosomal Dominant 30 MNT219 MRD30
Mental Retardation, Autosomal Dominant 31 MNT226 MRD31
Mental Retardation, Autosomal Dominant 32 MNT241 MRD32
Mental Retardation, Autosomal Dominant 33 MNT240 MRD33
Mental Retardation, Autosomal Dominant 34 MNT238 MRD34
Mental Retardation, Autosomal Dominant 35 MNT239 MRD35
Mental Retardation, Autosomal Dominant 36 MNT245 MRD36
Mental Retardation, Autosomal Dominant 38 MNT246 MRD38
Mental Retardation, Autosomal Dominant 39 MNT236 MRD39
Mental Retardation, Autosomal Dominant 40 MNT242 MRD40
Mental Retardation, Autosomal Dominant 41 MNT272 MRD41
Mental Retardation, Autosomal Dominant 42 MNT262 MRD42
Mental Retardation, Autosomal Dominant 43 MNT280 MRD43
Mental Retardation, Autosomal Dominant 44 MNT273 MRD44
Mental Retardation, Autosomal Dominant 45 MNT286 MRD45
Mental Retardation, Autosomal Dominant 46 MNT278 MRD46
Mental Retardation, Autosomal Dominant 47 MNT279 MRD47
Mental Retardation, Autosomal Dominant 48 MNT323 MRD48
Mental Retardation, Autosomal Dominant 49 MNT324 MRD49
Mental Retardation, Autosomal Dominant 50 MNT326 MRD50
Mental Retardation, Autosomal Dominant 51 MNT327 MRD51
Mental Retardation, Autosomal Dominant 52 MNT328 MRD52
Mental Retardation, Autosomal Dominant 53 MNT329 MRD53
Mental Retardation, Autosomal Dominant 54 MNT330 MRD54
Mental Retardation, Autosomal Dominant 55, with Seizures MNT331 MRD55
Mental Retardation, Autosomal Dominant 56 MNT332 MRD56
Mental Retardation, Autosomal Dominant 57 MNT334 MRD57
Mental Retardation, Autosomal Dominant 58 MNT337 MRD58
Mental Retardation, Autosomal Dominant 6, with or Without Seizures MNT320 MRD6
Mental Retardation, Autosomal Dominant 7 MNT185 MRD7
Mental Retardation, Autosomal Recessive 14 MNT154 MRT14
Mental Retardation, Autosomal Recessive 15 MNT150 MRT15
Mental Retardation, Autosomal Recessive 16 MNT167 MRT16
Mental Retardation, Autosomal Recessive 18 MNT151 MRT18
Mental Retardation, Autosomal Recessive 19 MNT182 MRT19
Mental Retardation, Autosomal Recessive 2 MNT155 MRT2
Mental Retardation, Autosomal Recessive 23 MNT170 MRT23
Mental Retardation, Autosomal Recessive 24 MNT162 MRT24
Mental Retardation, Autosomal Recessive 25 MNT172 MRT25
Mental Retardation, Autosomal Recessive 27 MNT177 MRT27
Mental Retardation, Autosomal Recessive 28 MNT165 MRT28
Mental Retardation, Autosomal Recessive 29 MNT161 MRT29
Mental Retardation, Autosomal Recessive 30 MNT163 MRT30
Mental Retardation, Autosomal Recessive 31 MNT160 MRT31
Mental Retardation, Autosomal Recessive 33 MNT180 MRT33
Mental Retardation, Autosomal Recessive 34, with Variant Lissencephaly MNT283 MRT34
Mental Retardation, Autosomal Recessive 35 MNT181 MRT35
Mental Retardation, Autosomal Recessive 36 MNT183 MRT36
Mental Retardation, Autosomal Recessive 37 MNT321 MRT37
Mental Retardation, Autosomal Recessive 38 MNT176 MRT38
Mental Retardation, Autosomal Recessive 39 MNT166 MRT39
Mental Retardation, Autosomal Recessive 40 MNT213 MRT40
Mental Retardation, Autosomal Recessive 41 MNT216 MRT41
Mental Retardation, Autosomal Recessive 42 MNT210 MRT42
Mental Retardation, Autosomal Recessive 43 MNT215 MRT43
Mental Retardation, Autosomal Recessive 44 MNT221 MRT44
Mental Retardation, Autosomal Recessive 45 MNT220 MRT45
Mental Retardation, Autosomal Recessive 46 MNT227 MRT46
Mental Retardation, Autosomal Recessive 47 MNT225 MRT47
Mental Retardation, Autosomal Recessive 48 MNT234 MRT48
Mental Retardation, Autosomal Recessive 49 MNT244 MRT49
Mental Retardation, Autosomal Recessive 5 MNT145 MRT5
Mental Retardation, Autosomal Recessive 50 MNT243 MRT50
Mental Retardation, Autosomal Recessive 51 MNT263 MRT51
Mental Retardation, Autosomal Recessive 52 MNT264 MRT52
Mental Retardation, Autosomal Recessive 53 MNT270 MRT53
Mental Retardation, Autosomal Recessive 54 MNT277 MRT54
Mental Retardation, Autosomal Recessive 55 MNT282 MRT55
Mental Retardation, Autosomal Recessive 56 MNT284 MRT56
Mental Retardation, Autosomal Recessive 57 MNT287 MRT57
Mental Retardation, Autosomal Recessive 58 MNT285 MRT58
Mental Retardation, Autosomal Recessive 59 MNT281 MRT59
Mental Retardation, Autosomal Recessive 60 MNT275 MRT60
Mental Retardation, Autosomal Recessive 61 MNT325 MRT61
Mental Retardation, Autosomal Recessive 63 MNT335 MRT63
Mental Retardation, Autosomal Recessive 64 MNT336 MRT64
Mental Retardation, Autosomal Recessive 65 MNT338 MRT65
Mental Retardation, Autosomal Recessive 66 MNT339 MRT66
Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma MNT317 MEDNIK
Mental Retardation, Fra12a Type MNT107
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism MNT315
Mental Retardation, Severe, with Spasticity and Pigmentary Tapetoretinal Degeneration MNT311 MRST
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy MNT252 MRSD
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome MNT318 MORMS
Mental Retardation, X-Linked 100 MNT223 MRX100
Mental Retardation, X-Linked 101 MNT224 MRX101
Mental Retardation, X-Linked 102 MNT248 MRX102
Mental Retardation, X-Linked 103 MNT289 MRX103
Mental Retardation, X-Linked 104 MNT267 MRX104
Mental Retardation, X-Linked 105 MNT274 MRX105
Mental Retardation, X-Linked 106 MNT294 MRX106
Mental Retardation, X-Linked 107 MNT333 MRX107
Mental Retardation, X-Linked 12 MNT305 MRX12
Mental Retardation, X-Linked 21 MNT301 MRX21
Mental Retardation, X-Linked 23 MNT204 MRX23
Mental Retardation, X-Linked 42 MNT205 MRX42
Mental Retardation, X-Linked 50 MNT194 MRX50
Mental Retardation, X-Linked 53 MNT202 MRX53
Mental Retardation, X-Linked 73 MNT247 MRX73
Mental Retardation, X-Linked 92 MNT196 MRX92
Mental Retardation, X-Linked 96 MNT195 MRX96
Mental Retardation, X-Linked 97 MNT200 MRX97
Mental Retardation, X-Linked 98 MNT198 MRX98
Mental Retardation, X-Linked 99 MNT218 MRX99
Mental Retardation, X-Linked 99, Syndromic, Female-Restricted MNT290 MRXS99F
Mental Retardation, X-Linked, Associated with Fragile Site Fraxe MNT307 MRFRAXE
Mental Retardation, X-Linked, Syndromic 13 MNT135 MRXS13
Mental Retardation, X-Linked, Syndromic 17 MNT191 MRXS17
Mental Retardation, X-Linked, Syndromic 32 MNT207 MRXS32
Mental Retardation, X-Linked, Syndromic 33 MNT295 MRXS33
Mental Retardation, X-Linked, Syndromic 34 MNT296 MRXS34
Mental Retardation, X-Linked, Syndromic 9 MNT197 MRXS9
Mental Retardation, X-Linked, Syndromic, 35 MNT298 MRXS35
Mental Retardation, X-Linked, Syndromic, Bain Type MNT269 MRXSB
Mental Retardation, X-Linked, Syndromic, Cabezas Type MNT303 MRXSC
Mental Retardation, X-Linked, Syndromic, Christianson Type MNT302 MRXSCH
Mental Retardation, X-Linked, Syndromic, Chudley-Schwartz Type MNT201 MRXSCS
Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type MNT228 MRXSCJ
Mental Retardation, X-Linked, Syndromic, Hedera Type MNT192 MRXSH
Mental Retardation, X-Linked, Syndromic, Houge Type MNT306 MRXSHG
Mental Retardation, X-Linked, Syndromic, Martin-Probst Type MNT146 MRXSMP
Mental Retardation, X-Linked, Syndromic, Nascimento Type MNT056 MRXSN
Mental Retardation, X-Linked, Syndromic, Raymond Type MNT057 MRXSR
Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type MNT310 MRXSSR
Mental Retardation, X-Linked, Syndromic, Turner Type MNT058 MRXST
Mental Retardation, X-Linked, Syndromic, Wu Type MNT258 MRXSW
Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance MNT229 MRXSO
Mental Retardation, X-Linked, with or Without Seizures, Arx-Related MNT304 MRXARX
Mental Retardation, X-Linked, with Panhypopituitarism MNT300 MRXGH
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 MNT309 MRXHF1
Mercaptolactate-Cysteine Disulfiduria MRC009 MCDU
Mercury Poisoning MRC003
Merkel Cell Carcinoma MRK001 MCC
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 MMDK
Mesomelic Dysplasia, Savarirayan Type MSM019
Mesothelioma, Malignant MST023 MESOM
Metabolic Acidosis MTB004
Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration MTB008 MECRCN
Metabolic Crises, Recurrent, with Variable Encephalomyopathic Features and Neurologic Regression MTB009 MECREN
Metabolic Myopathy MTB016
Metacarpal 4-5 Fusion MTC100 MF4
Metachondromatosis MTC018 METCDS
Metachromatic Leukodystrophy MTC003 MLD
Metachromatic Leukodystrophy Due to Saposin B Deficiency MTC019 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, Jansen Type MTP034 MCDJ
Metaphyseal Chondrodysplasia, Schmid Type MTP025 MCDS
Metaphyseal Dysplasia Maxillary Hypoplasia Brachydactyly MTP010
Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly MTP023 MDMHB
Metaphyseal Dysplasia Without Hypotrichosis MTP003 MDWH
Metaphyseal Dysplasia, Spahr Type MTP028 MDST
Metaphyseal Enchondromatosis with D-2-Hydroxyglutaric Aciduria MTP033
Metaphyseal Undermodeling, Spondylar Dysplasia, and Overgrowth MTP011
Metatarsus Adductus MTT004
Metatropic Dysplasia MTT002 MTD
Metatypical Basal Cell Carcinoma MTT001
Methane Production MTH071
Methanol Poisoning MTH047
Methemoglobin Reductase Deficiency MTH072
Methemoglobinemia MTH007
Methemoglobinemia and Ambiguous Genitalia MTH082 METAG
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase MTH026 METHB-CYB5R3
Methemoglobinemia, Alpha Type MTH084
Methemoglobinemia, Beta Type MTH083
Methemoglobinemia, Beta-Globin Type MTH064
Methionine Adenosyltransferase Deficiency MTH011
Methionine Adenosyltransferase I/iii Deficiency MTH074 MATD
Methotrexate Toxicity or Dose Selection MTH061
Methylmalonate Semialdehyde Dehydrogenase Deficiency MTH013 MMSDHD
Methylmalonic Acidemia MTH008 MMA
Methylmalonic Acidemia and Homocysteinemia, Cblx Type MTH079 MRX3
Methylmalonic Acidemia with Homocystinuria MTH021
Methylmalonic Aciduria and Homocystinuria Type Cble MTH003
Methylmalonic Aciduria and Homocystinuria Type Cblg MTH002
Methylmalonic Aciduria and Homocystinuria, Cblc Type MTH054 MAHCC
Methylmalonic Aciduria and Homocystinuria, Cbld Type MTH055 MAHCD
Methylmalonic Aciduria and Homocystinuria, Cblf Type MTH056 MAHCF
Methylmalonic Aciduria and Homocystinuria, Cblj Type MTH051 MAHCJ
Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency MTH076 MMAM
Methylmalonic Aciduria, Cbla Type MTH077 MMAA
Methylmalonic Aciduria, Cblb Type MTH078 MMAB
Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect MTH068 MMATC
Methylmalonyl-Coa Epimerase Deficiency MTH040 MCEED
Methylmalonyl-Coenzyme a Mutase Deficiency MTH025
Metopic Ridging-Ptosis-Facial Dysmorphism Syndrome MTP038
Mevalonic Aciduria MVL001 MEVA
Microcephalic Osteodysplastic Primordial Dwarfism, Type I MCR240 MOPD1
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 18, Primary, Autosomal Dominant MCR322 MCPH18
Microcephaly 19, Primary, Autosomal Recessive MCR356 MCPH19
Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations MCR222 MCPH2
Microcephaly 20, Primary, Autosomal Recessive MCR360 MCPH20
Microcephaly 21, Primary, Autosomal Recessive MCR361 MCPH21
Microcephaly 22, Primary, Autosomal Recessive MCR362 MCPH22
Microcephaly 23, Primary, Autosomal Recessive MCR363 MCPH23
Microcephaly 24, Primary, Autosomal Recessive MCR368 MCPH24
Microcephaly 25, Primary, Autosomal Recessive MCR372 MCPH25
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 Simplified Gyral Pattern MCR345
Microcephaly with Spastic Quadriplegia MCR060
Microcephaly, Amish Type MCR257 MCPHA
Microcephaly, Autosomal Dominant MCR329
Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum MCR369 MCIDDS
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis MCR315 MCCPD
Microcephaly, Epilepsy, and Diabetes Syndrome MCR209 MEDS
Microcephaly, Facial Dysmorphism, Renal Agenesis, and Ambiguous Genitalia Syndrome MCR366 MFRG
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations MCR371 MIGSB
Microcephaly, Growth Restriction, and Increased Sister Chromatid Exchange 2 MCR365 MGRISCE2
Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy MCR123 MCPHSBA
Microcephaly, Progressive, with Seizures and Cerebral and Cerebellar Atrophy MCR355 MSCCA
Microcephaly, Seizures, and Developmental Delay MCR064 MCSZ
Microcephaly, Seizures, Spasticity, and Brain Calcifications MCR333 MISSBC
Microcephaly, Short Stature, and Impaired Glucose Metabolism 1 MCR323 MSSGM1
Microcephaly, Short Stature, and Impaired Glucose Metabolism 2 MCR316 MSSGM2
Microcephaly, Short Stature, and Limb Abnormalities MCR327 MISSLA
Microcephaly, Short Stature, and Polymicrogyria with or Without Seizures MCR354 MSSP
Microcephaly-Capillary Malformation Syndrome MCR183 MICCAP
Microcephaly-Complex Motor and Sensory Axonal Neuropathy Syndrome MCR298
Microcephaly-Corpus Callosum and Cerebellar Vermis Hypoplasia-Facial Dysmorphism-Intellectual Disability Syndrom MCR358
Microcephaly-Facial Dysmorphism-Ocular Anomalies-Multiple Congenital Anomalies Syndrome MCR367
Microcephaly-Micromelia Syndrome MCR326 MIMIS
Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome MCR285
Microcephaly-Short Stature-Intellectual Disability-Facial Dysmorphism Syndrome MCR280
Microcolon MCR334
Microcoria, Congenital MCR067 MCOR
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus MCR220 MMCAT
Microcystic Adenoma MCR014
Microcystic Meningioma MCR001
Microcytic Anemia MCR018
Microencephaly MCR374
Microform Holoprosencephaly MCR173 HPE-L
Microglandular Adenosis MCR019
Microhydranencephaly MCR025 MHAC
Microinvasive Cervical Squamous Cell Carcinoma MCR015
Microinvasive Gastric Cancer MCR011
Microlissencephaly MCR099
Microphthalmia MCR013
Microphthalmia with Limb Anomalies MCR165 MLA
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 Cataract 1 MCR330 MCOPCT1
Microphthalmia, Isolated, with Coloboma 1 MCR338 MCOPCB1
Microphthalmia, Isolated, with Coloboma 10 MCR271 MCOPCB10
Microphthalmia, Isolated, with Coloboma 2 MCR346 MCOPCB2
Microphthalmia, Isolated, with Coloboma 3 MCR349 MCOPCB3
Microphthalmia, Isolated, with Coloboma 5 MCR350 MCOPCB5
Microphthalmia, Isolated, with Coloboma 6 MCR352 MCOPCB6
Microphthalmia, Isolated, with Coloboma 7 MCR210 MCOPCB7
Microphthalmia, Isolated, with Coloboma 9 MCR214 MCOPCB9
Microphthalmia, Syndromic 1 MCR263 MCOPS1
Microphthalmia, Syndromic 11 MCR217 MCOPS11
Microphthalmia, Syndromic 12 MCR212 MCOPS12
Microphthalmia, Syndromic 13 MCR228 MCOPS13
Microphthalmia, Syndromic 2 MCR261 MCOPS2
Microphthalmia, Syndromic 3 MCR241 MCOPS3
Microphthalmia, Syndromic 4 MCR262 MCOPS4
Microphthalmia, Syndromic 5 MCR252 MCOPS5
Microphthalmia, Syndromic 6 MCR251 MCOPS6
Microphthalmia, Syndromic 8 MCR245 MCOPS8
Microphthalmia, Syndromic 9 MCR256 MCOPS9
Microphthalmia/anophthalmia/coloboma Spectrum MCR273
Microphthalmia/coloboma and Skeletal Dysplasia Syndrome MCR324 MCSKS
Microscopic 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 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
Mid-Dermal Elastolysis MDD015
Middle Cerebral Artery Infarction MDD003
Middle Ear Adenoma MDD008
Middle Ear Carcinoma MDD009
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 MGR7
Migraine with Aura 9 MGR027 MGR9
Migraine with Brainstem Aura MGR035 MBA
Migraine with or Without Aura 1 MGR028 MA
Migraine with or Without Aura 12 MGR040 MGR12
Migraine with or Without Aura 13 MGR042 MGR13
Migraine with or Without Aura 2 MGR036 MFTS
Migraine with or Without Aura 3 MGR022 MGR3
Migraine with or Without Aura 5 MGR024 MGR5
Migraine with or Without Aura 6 MGR033 MGR6
Migraine with or Without Aura 8 MGR037 MGR8
Migraine Without Aura MGR001
Migraine Without Aura 4 MGR023 MGOA
Migraine, Familial Hemiplegic, 1 MGR032 FHM1
Migraine, Familial Hemiplegic, 2 MGR030 FHM2
Migraine, Familial Hemiplegic, 3 MGR031 FHM3
Mikulicz Disease MKL001
Mild Hyperphenylalaninemia MLD011 MHPA
Mild Phenylketonuria MLD010 MPKU
Mild Pre-Eclampsia MLD002
Miles-Carpenter Syndrome MLS013 MCS
Miliaria MLR009
Miliaria Rubra MLR001
Miliary Tuberculosis MLR002
Milk Allergy MLK006
Milker's Nodule MLK001
Miller Fisher Syndrome MLL002
Miller-Dieker Lissencephaly Syndrome MLL018 MDLS
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
Mirror Movements 4 MRR015 MRMV4
Mismatch Repair Cancer Syndrome MSM014 MMRCS
Mitchell-Riley Syndrome MTC096 MTCHRS
Mite Infestation MTN002
Mitochondrial Complex I Deficiency, Mitochondrial Type 1 MTC149 MC1DM1
Mitochondrial Complex I Deficiency, Nuclear Type 1 MTC146 MC1DN1
Mitochondrial Complex I Deficiency, Nuclear Type 10 MTC158 MC1DN10
Mitochondrial Complex I Deficiency, Nuclear Type 11 MTC159 MC1DN11
Mitochondrial Complex I Deficiency, Nuclear Type 12 MTC147 MC1DN12
Mitochondrial Complex I Deficiency, Nuclear Type 13 MTC160 MC1DN13
Mitochondrial Complex I Deficiency, Nuclear Type 14 MTC161 MC1DN14
Mitochondrial Complex I Deficiency, Nuclear Type 15 MTC162 MC1DN15
Mitochondrial Complex I Deficiency, Nuclear Type 16 MTC163 MC1DN16
Mitochondrial Complex I Deficiency, Nuclear Type 17 MTC164 MC1DN17
Mitochondrial Complex I Deficiency, Nuclear Type 18 MTC165 MC1DN18
Mitochondrial Complex I Deficiency, Nuclear Type 19 MTC166 MC1DN19
Mitochondrial Complex I Deficiency, Nuclear Type 2 MTC152 MC1DN2
Mitochondrial Complex I Deficiency, Nuclear Type 20 MTC151 MC1DN20
Mitochondrial Complex I Deficiency, Nuclear Type 21 MTC167 MC1DN21
Mitochondrial Complex I Deficiency, Nuclear Type 22 MTC168 MC1DN22
Mitochondrial Complex I Deficiency, Nuclear Type 23 MTC169 MC1DN23
Mitochondrial Complex I Deficiency, Nuclear Type 24 MTC170 MC1DN24
Mitochondrial Complex I Deficiency, Nuclear Type 25 MTC171 MC1DN25
Mitochondrial Complex I Deficiency, Nuclear Type 26 MTC172 MC1DN26
Mitochondrial Complex I Deficiency, Nuclear Type 27 MTC173 MC1DN27
Mitochondrial Complex I Deficiency, Nuclear Type 28 MTC174 MC1DN28
Mitochondrial Complex I Deficiency, Nuclear Type 29 MTC175 MC1DN29
Mitochondrial Complex I Deficiency, Nuclear Type 30 MTC148 MC1DN30
Mitochondrial Complex I Deficiency, Nuclear Type 31 MTC176 MC1DN31
Mitochondrial Complex I Deficiency, Nuclear Type 32 MTC177 MC1DN32
Mitochondrial Complex I Deficiency, Nuclear Type 33 MTC178 MC1DN33
Mitochondrial Complex I Deficiency, Nuclear Type 4 MTC153 MC1DN4
Mitochondrial Complex I Deficiency, Nuclear Type 6 MTC154 MC1DN6
Mitochondrial Complex I Deficiency, Nuclear Type 7 MTC155 MC1DN7
Mitochondrial Complex I Deficiency, Nuclear Type 8 MTC156 MC1DN8
Mitochondrial Complex I Deficiency, Nuclear Type 9 MTC157 MC1DN9
Mitochondrial Complex Ii Deficiency MTC020 MT-C2D
Mitochondrial Complex Iii Deficiency MTC008
Mitochondrial Complex Iii Deficiency, Nuclear Type 1 MTC085 MC3DN1
Mitochondrial Complex Iii Deficiency, Nuclear Type 2 MTC091 MC3DN2
Mitochondrial Complex Iii Deficiency, Nuclear Type 3 MTC089 MC3DN3
Mitochondrial Complex Iii Deficiency, Nuclear Type 4 MTC087 MC3DN4
Mitochondrial Complex Iii Deficiency, Nuclear Type 6 MTC090 MC3DN6
Mitochondrial Complex Iii Deficiency, Nuclear Type 7 MTC095 MC3DN7
Mitochondrial Complex Iii Deficiency, Nuclear Type 8 MTC094 MC3DN8
Mitochondrial Complex Iii Deficiency, Nuclear Type 9 MTC098 MC3DN9
Mitochondrial Complex Iv Deficiency MTC097 MT-C4D
Mitochondrial Complex V Deficiency, Mitochondrial Type 1 MTC150 MC5DM1
Mitochondrial Complex V Deficiency, Nuclear Type 1 MTC029 MC5DN1
Mitochondrial Complex V Deficiency, Nuclear Type 2 MTC068 MC5DN2
Mitochondrial Complex V Deficiency, Nuclear Type 3 MTC030 MC5DN3
Mitochondrial Complex V Deficiency, Nuclear Type 4 MTC137 MC5DN4
Mitochondrial Complex V Deficiency, Nuclear Type 5 MTC141 MC5DN5
Mitochondrial Disease with Epilepsy MTC196
Mitochondrial Disease with Hypertrophic Cardiomyopathy MTC194
Mitochondrial Disorders MTC069
Mitochondrial Dna Deletion Syndromes MTC014
Mitochondrial Dna Depletion Syndrome MTC010
Mitochondrial Dna Depletion Syndrome 1 MTC061 MTDPS1
Mitochondrial Dna Depletion Syndrome 11 MTC078 MTDPS11
Mitochondrial Dna Depletion Syndrome 12a MTC142
Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant MTC139 MTDPS12A
Mitochondrial Dna Depletion Syndrome 12b MTC143
Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive MTC138 MTDPS12B
Mitochondrial Dna Depletion Syndrome 13 MTC088 MTDPS13
Mitochondrial Dna Depletion Syndrome 14 MTC126 MTDPS14
Mitochondrial Dna Depletion Syndrome 15 MTC129 MTDPS15
Mitochondrial Dna Depletion Syndrome 16 MTC182 MTDPS16
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, Encephalomyopathic Form with Methylmalonic Aciduria MTC144
Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form Due to Dguok Deficiency MTC103
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form MTC093
Mitochondrial Dna Maintenance Defects MTC140
Mitochondrial Dna-Associated Leigh Syndrome MTC112 MILS
Mitochondrial Dna-Associated Leigh Syndrome and Narp MTC015
Mitochondrial Dna-Related Cardiomyopathy and Hearing Loss MTC179
Mitochondrial Dna-Related Progressive External Ophthalmoplegia MTC181
Mitochondrial Encephalomyopathy MTC004
Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes MTC023 MELAS
Mitochondrial Membrane Protein-Associated Neurodegeneration MTC036 MPAN
Mitochondrial Metabolism Disease MTC005
Mitochondrial Myopathy MTC133
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, Episodic, with or Without Optic Atrophy and Reversible Leukoencephalopathy MTC145 MEOAL
Mitochondrial Myopathy, Infantile, Transient MTC116 MMIT
Mitochondrial Myopathy, Lethal, Infantile MTC115 LIMM
Mitochondrial Neurogastrointestinal Encephalomyopathy MTC111 MNGIE
Mitochondrial Non-Syndromic Sensorineural Deafness MTC106
Mitochondrial Oxidative Phosphorylation Disorder MTC195
Mitochondrial Phosphate Carrier Deficiency MTC037 MPCD
Mitochondrial Pyruvate Carrier Deficiency MTC079 MPYCD
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency MTC108 ECHS1D
Mitochondrial Trifunctional Protein Deficiency MTC027 MTPD
Mitral Atresia MTR027
Mitral Valve Disease MTR012
Mitral Valve Insufficiency MTR002
Mitral Valve Prolapse 1 MTR080 MVP1
Mitral Valve Prolapse 2 MTR077 MVP2
Mitral Valve Prolapse 3 MTR083 MVP3
Mitral Valve Stenosis MTR003
Mixed Cell Adenoma MXD020
Mixed Cell Type Cancer MXD023
Mixed Cell Uveal Melanoma MXD040
Mixed Cerebral Palsy MXD001
Mixed Connective Tissue Disease MXD005 MCTD
Mixed Ductal-Endocrine Carcinoma MXD014
Mixed Endometrial Stromal and Smooth Muscle Tumor MXD017
Mixed Epithelial Stromal Tumour MXD010
Mixed Fibrolamellar Hepatocellular Carcinoma MXD042
Mixed Germ Cell Cancer MXD025
Mixed Germ Cell Tumor MXD032
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 Neuronal-Glial Tumor MXD046
Mixed Oligodendroglioma-Astrocytoma MXD012
Mixed Sleep Apnea MXD044
Mixed Type Thymoma MXD027
Miyoshi Muscular Dystrophy MYS079
Miyoshi Muscular Dystrophy 1 MYS033 MMD1
Miyoshi Muscular Dystrophy 2 MYS019 MMD2
Miyoshi Muscular Dystrophy 3 MYS014 MMD3
Moderate and Severe Traumatic Brain Injury MDR006
Moebius Syndrome MBS002 MBS
Mohr Syndrome MHR002 OFD2
Mohr-Tranebjaerg Syndrome MHR001 MTS
Molluscum Contagiosum MLL001
Molybdenum Cofactor Deficiency MLY001 MOCOD
Molybdenum Cofactor Deficiency, Complementation Group a MLY008 MOCODA
Molybdenum Cofactor Deficiency, Complementation Group B MLY009 MOCODB
Molybdenum Cofactor Deficiency, Complementation Group C MLY010 MOCODC
Momo Syndrome MMS001
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
Mononeuritis Multiplex MNN002
Mononeuritis of Lower Limb MNN015
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 7 of Bone Marrow MNS016 MLSM7
Monosomy 9q22.3 MNS011
Monostotic Fibrous Dysplasia MNS012
Mood Disorder MDD011
Mooren's Ulcer MRN002
Morbid Obesity and Spermatogenic Failure MRB006 MOSPGF
Morgagni Cataract MRG001
Morpheaform Basal Cell Carcinoma MRP002
Morphine Dependence MRP001
Morquio Syndrome MRQ003
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
Mosaic Variegated Aneuploidy Syndrome 3 MSC139 MVA3
Motion Sickness MTN003
Motor Neuron Disease MTR014
Motor Peripheral Neuropathy MTR007 HSMN
Motor Stereotypies MTR086
Mouth Disease MTH009
Movement Disease MVM001
Mowat-Wilson Syndrome MWT001 MOWS
Moyamoya Angiopathy MYM016
Moyamoya Disease 1 MYM013 MYMY1
Moyamoya Disease 2 MYM004 MYMY2
Moyamoya Disease 3 MYM005 MYMY3
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism MYM012 MYMY4
Moyamoya Disease 5 MYM003 MYMY5
Moyamoya Disease 6 with or Without Achalasia MYM015 MYMY6
Mpv17-Related Mitochondrial Dna Maintenance Defect MPV002
Mt-Atp6-Related Mitochondrial Spastic Paraplegia MTT008
Mthfr Gene Variant MTH081
Mu Chain Disease MCH003
Mucinoses MCN011
Mucinous Adenocarcinoma MCN001
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
Muckle-Wells Syndrome MCK007 MWS
Mucocele of Appendix MCC004
Mucocele of Salivary Gland MCC003
Mucocutaneous Leishmaniasis MCC002
Mucocutaneous Ulceration, Chronic MCC013 CMCU
Mucoepidermoid Carcinoma MCP006 MEC
Mucoepidermoid Esophageal Carcinoma MCP008
Mucolipidoses MCL022
Mucolipidosis MCL001
Mucolipidosis Ii Alpha/beta MCL062 MLII
Mucolipidosis Iii Alpha/beta MCL046 MLIIIA
Mucolipidosis Iii Gamma MCL016 MLIIIC
Mucolipidosis Iv MCL013 ML4
Mucopolysaccharidoses MCP033
Mucopolysaccharidosis Iii MCP001 MPS3
Mucopolysaccharidosis Type 2, Attenuated Form MCP034
Mucopolysaccharidosis Type 2, Severe Form MCP035
Mucopolysaccharidosis Type 6, Rapidly Progressing MCP029
Mucopolysaccharidosis Type 6, Slowly Progressing MCP028
Mucopolysaccharidosis, Type Ii MCP050 MPS2
Mucopolysaccharidosis, Type Iiia MCP043 MPS3A
Mucopolysaccharidosis, Type Iiib MCP044 MPS3B
Mucopolysaccharidosis, Type Iiic MCP045 MPS3C
Mucopolysaccharidosis, Type Iiid MCP046 MPS3D
Mucopolysaccharidosis, Type Iva MCP047 MPS4A
Mucopolysaccharidosis, Type Ivb MCP048 MPS4B
Mucopolysaccharidosis, Type Ix MCP051 MPS9
Mucopolysaccharidosis, Type Vi MCP052 MPS6
Mucopolysaccharidosis, Type Vii MCP049 MPS7
Mucopolysaccharidosis-Plus Syndrome MCP040 MPSPS
Mucormycosis MCR141
Mucosal Melanoma MCS004
Mucositis MCS002
Muenke Syndrome MNK003 MNKES
Muir-Torre Syndrome MRT001 MRTES
Mulchandani-Bhoj-Conlin Syndrome MLC004 MBCS
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, Nodulosis, and Arthropathy MLT065 MONA
Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum MLT138
Multicentric Papillary Thyroid Carcinoma MLT005
Multicentric Reticulohistiocytosis MLT016
Multicore Disease MLT168
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
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly MLT161 MARCH
Multiple Acyl-Coa Dehydrogenase Deficiency MLT118 MADD
Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type MLT154
Multiple Acyl-Coa Dehydrogenase Deficiency, Severe Neonatal Type MLT155
Multiple Benign Circumferential Skin Creases on Limbs MLT104 CCSF
Multiple Carboxylase Deficiency MLT018 MCD
Multiple Chemical Sensitivity MLT001
Multiple Congenital Anomalies/dysmorphic Syndrome-Intellectual Disability MLT173
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome MLT140
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1 MLT126 MCAHS1
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 MLT128 MCAHS2
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 MLT127 MCAHS3
Multiple Cranial Nerve Palsy MLT009
Multiple Enchondromatosis, Maffucci Type MLT145
Multiple Endocrine Neoplasia MLT074 MEA
Multiple Endocrine Neoplasia, Type I MLT156 MEN1
Multiple Endocrine Neoplasia, Type Iia MLT160 MEN2A
Multiple Endocrine Neoplasia, Type Iib MLT159 MEN2B
Multiple Endocrine Neoplasia, Type Iv MLT086 MEN4
Multiple Epiphyseal Dysplasia MLT007 EDM
Multiple Epiphyseal Dysplasia and Pseudoachondroplasia MLT171
Multiple Epiphyseal Dysplasia Due to Collagen 9 Anomaly MLT141
Multiple Epiphyseal Dysplasia, Autosomal Dominant MLT142
Multiple Epiphyseal Dysplasia, Recessive MLT031 EDM4
Multiple Familial Trichoepithelioma MLT048 EAC
Multiple Fibroadenomas of the Breast MLT120 MFAB
Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects MLT162 JDSCD
Multiple Mitochondrial Dysfunctions Syndrome MLT027 MMDS
Multiple Mitochondrial Dysfunctions Syndrome 1 MLT068 MMDS1
Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia MLT150 MMDS2
Multiple Mitochondrial Dysfunctions Syndrome 3 MLT119 MMDS3
Multiple Mitochondrial Dysfunctions Syndrome 4 MLT139 MMDS4
Multiple Mitochondrial Dysfunctions Syndrome 5 MLT151 MMDS5
Multiple Mitochondrial Dysfunctions Syndrome 6 MLT167 MMDS6
Multiple Mucosal Neuroma MLT011
Multiple Paragangliomas Associated with Polycythemia MLT106
Multiple Personality Disorder MLT010
Multiple Pterygium Syndrome, Escobar Variant MLT163 EVMPS
Multiple Pterygium Syndrome, Lethal Type MLT134 LMPS
Multiple Sclerosis MLT020 MS
Multiple Sclerosis 2 MLT093 MS2
Multiple Sclerosis 3 MLT094 MS3
Multiple Sclerosis 4 MLT095 MS4
Multiple Sclerosis 5 MLT124 MS5
Multiple Self-Healing Squamous Epithelioma MLT152 MSSE
Multiple Sulfatase Deficiency MLT135 MSD
Multiple Synostoses Syndrome MLT072
Multiple Synostoses Syndrome 1 MLT059 SYNS1
Multiple Synostoses Syndrome 2 MLT060 SYNS2
Multiple Synostoses Syndrome 3 MLT078 SYNS3
Multiple Synostoses Syndrome 4 MLT166 SYNS4
Multiple System Atrophy 1 MLT157 MSA1
Multiple System Atrophy, 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 Eye Brain Disease MSC077 MEB
Muscle Hypertrophy MSC007 MSLHP
Muscle Strength Quantitative Trait Locus 1 MSC054
Muscle Tissue Disease MSC004
Muscular Atrophy MSC003
Muscular Disease MSC190
Muscular Dystrophy MSC005
Muscular Dystrophy, Autosomal Recessive, with Cardiomyopathy and Triangular Tongue MSC185 MDRCMTT
Muscular Dystrophy, Becker Type MSC152 BMD
Muscular Dystrophy, Congenital Merosin-Deficient, 1a MSC162 MDC1A
Muscular Dystrophy, Congenital, 1b MSC050 MDC1B
Muscular Dystrophy, Congenital, Davignon-Chauveau Type MSC141 MDCDC
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency MSC164 MDCI
Muscular Dystrophy, Congenital, Lmna-Related MSC165 MDCL
Muscular Dystrophy, Congenital, Megaconial Type MSC028 MDCMC
Muscular Dystrophy, Congenital, Merosin-Positive MSC029
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability MSC142 MDCCAID
Muscular Dystrophy, Duchenne Type MSC157 DMD
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 MSC175 LGMDD1
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2 MSC178 LGMDD2
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 MSC180 LGMDD3
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 4 MSC187 LGMDD4
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 MSC169 LGMDR1
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 MSC179 LGMDR10
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 12 MSC181 LGMDR12
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 17 MSC183 LGMDR17
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 18 MSC184 LGMDR18
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 MSC170 LGMDR2
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 21 MSC186 LGMDR21
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 23 MSC189 LGMDR23
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 25 MSC191 LGMDR25
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 MSC177 LGMDR3
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 MSC176 LGMDR4
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 MSC171 LGMDR5
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 MSC173 LGMDR6
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7 MSC174 LGMDR7
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 MSC172 LGMDR8
Muscular Dystrophy, Limb-Girdle, Type 1h MSC058 LGMD1H
Muscular Dystrophy-Dystroglycanopathy MSC002
Muscular Dystrophy-Dystroglycanopathy , Type a, 1 MSC047 MDDGA1
Muscular Dystrophy-Dystroglycanopathy , Type a, 10 MSC107 MDDGA10
Muscular Dystrophy-Dystroglycanopathy , Type a, 11 MSC167 MDDGA11
Muscular Dystrophy-Dystroglycanopathy , Type a, 12 MSC102 MDDGA12
Muscular Dystrophy-Dystroglycanopathy , Type a, 13 MSC105 MDDGA13
Muscular Dystrophy-Dystroglycanopathy , Type a, 14 MSC097 MDDGA14
Muscular Dystrophy-Dystroglycanopathy , Type a, 2 MSC043 MDDGA2
Muscular Dystrophy-Dystroglycanopathy , Type a, 3 MSC045 MDDGA3
Muscular Dystrophy-Dystroglycanopathy , Type a, 4 MSC037 MDDGA4
Muscular Dystrophy-Dystroglycanopathy , Type a, 5 MSC034 MDDGA5
Muscular Dystrophy-Dystroglycanopathy , Type a, 6 MSC041 MDDGA6
Muscular Dystrophy-Dystroglycanopathy , Type a, 7 MSC101 MDDGA7
Muscular Dystrophy-Dystroglycanopathy , Type a, 8 MSC166 MDDGA8
Muscular Dystrophy-Dystroglycanopathy , Type a, 9 MSC127 MDDGA9
Muscular Dystrophy-Dystroglycanopathy , Type B, 1 MSC048 MDDGB1
Muscular Dystrophy-Dystroglycanopathy , Type B, 14 MSC099 MDDGB14
Muscular Dystrophy-Dystroglycanopathy , Type B, 2 MSC044 MDDGB2
Muscular Dystrophy-Dystroglycanopathy , Type B, 3 MSC046 MDDGB3
Muscular Dystrophy-Dystroglycanopathy , Type B, 4 MSC038 MDDGB4
Muscular Dystrophy-Dystroglycanopathy , Type B, 5 MSC035 MDDGB5
Muscular Dystrophy-Dystroglycanopathy , Type B, 6 MSC042 MDDGB6
Muscular Dystrophy-Dystroglycanopathy , Type C, 1 MSC104 MDDGC1
Muscular Dystrophy-Dystroglycanopathy , Type C, 12 MSC118 MDDGC12
Muscular Dystrophy-Dystroglycanopathy , Type C, 14 MSC098 MDDGC14
Muscular Dystrophy-Dystroglycanopathy , Type C, 15 MSC182 MDDGC15
Muscular Dystrophy-Dystroglycanopathy , Type C, 2 MSC108 MDDGC2
Muscular Dystrophy-Dystroglycanopathy , Type C, 3 MSC093 MDDGC3
Muscular Dystrophy-Dystroglycanopathy , Type C, 4 MSC103 MDDGC4
Muscular Dystrophy-Dystroglycanopathy , Type C, 5 MSC036 MDDGC5
Muscular Dystrophy-Dystroglycanopathy , Type C, 7 MSC111 MDDGC7
Muscular Dystrophy-Dystroglycanopathy , Type C, 8 MSC188 MDDGC8
Muscular Dystrophy-Dystroglycanopathy , Type C, 9 MSC100 MDDGC9
Muscular Glycogenosis MSC192
Muscular Lipidosis MSC193
Muscular Phosphorylase Kinase Deficiency MSC031
Musculocontractural Ehlers-Danlos Syndrome MSC134 MCEDS
Musical Aptitude Quantitative Trait Locus MSC163
Mutagen Sensitivity MTG002
Mutism MTS001
Mutyh-Associated Polyposis MTY001
Myasthenia Gravis MYS003 MG
Myasthenia Gravis Congenital MYS011
Myasthenia Gravis with Thymus Hyperplasia MYS007 MYAS1
Myasthenic Syndrome, Congenital, 10 MYS052 CMS10
Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency MYS057 CMS11
Myasthenic Syndrome, Congenital, 12 MYS074 CMS12
Myasthenic Syndrome, Congenital, 13 MYS075 CMS13
Myasthenic Syndrome, Congenital, 14 MYS078 CMS14
Myasthenic Syndrome, Congenital, 15 MYS077 CMS15
Myasthenic Syndrome, Congenital, 16 MYS064 CMS16
Myasthenic Syndrome, Congenital, 17 MYS056 CMS17
Myasthenic Syndrome, Congenital, 18 MYS065 CMS18
Myasthenic Syndrome, Congenital, 19 MYS070 CMS19
Myasthenic Syndrome, Congenital, 1a, Slow-Channel MYS046 CMS1A
Myasthenic Syndrome, Congenital, 1b, Fast-Channel MYS047 CMS1B
Myasthenic Syndrome, Congenital, 20, Presynaptic MYS068 CMS20
Myasthenic Syndrome, Congenital, 21, Presynaptic MYS069 CMS21
Myasthenic Syndrome, Congenital, 22 MYS067 CMS22
Myasthenic Syndrome, Congenital, 23, Presynaptic MYS080 CMS23
Myasthenic Syndrome, Congenital, 24, Presynaptic MYS081 CMS24
Myasthenic Syndrome, Congenital, 25, Presynaptic MYS082 CMS25
Myasthenic Syndrome, Congenital, 2a, Slow-Channel MYS062 CMS2A
Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency MYS063 CMS2C
Myasthenic Syndrome, Congenital, 3a, Slow-Channel MYS048 CMS3A
Myasthenic Syndrome, Congenital, 3b, Fast-Channel MYS049 CMS3B
Myasthenic Syndrome, Congenital, 3c, Associated with Acetylcholine Receptor Deficiency MYS050 CMS3C
Myasthenic Syndrome, Congenital, 4a, Slow-Channel MYS059 CMS4A
Myasthenic Syndrome, Congenital, 4b, Fast-Channel MYS060 CMS4B
Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency MYS061 CMS4C
Myasthenic Syndrome, Congenital, 5 MYS051 CMS5
Myasthenic Syndrome, Congenital, 6, Presynaptic MYS055 CMS6
Myasthenic Syndrome, Congenital, 7, Presynaptic MYS044 CMS7
Myasthenic Syndrome, Congenital, 8 MYS076 CMS8
Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency MYS054 CMS9
Mybpc1-Related Autosomal Recessive Non-Lethal Arthrogryposis Multiplex Congenita Syndrome MYB004
Mycetoma MYC012
Mycobacterium Abscessus MYC013
Mycobacterium Chelonae MYC014
Mycobacterium Fortuitum MYC015
Mycobacterium Gordonae MYC016
Mycobacterium Kansasii MYC017
Mycobacterium Malmoense MYC018
Mycobacterium Marinum MYC019
Mycobacterium Tuberculosis 1 MYC084 TB
Mycobacterium Tuberculosis 2 MYC054 MTBS2
Mycobacterium Tuberculosis 3 MYC055 MTBS3
Mycobacterium Tuberculosis X-Linked MYC081 MTBSX
Mycobacterium Tuberculosis, Susceptibility to Infection by MYC020
Mycoplasma Pneumoniae Pneumonia MYC087
Mycosis Fungoides MYC006
Myd88 Deficiency MYD002 MYD88D
Myelitis MYL001
Myelocystocele MYL044
Myelodysplastic Syndrome MYL009 MDS
Myelodysplastic Syndrome with Excess Blasts MYL074 RAEB
Myelodysplastic/myeloproliferative Neoplasm MYL075
Myelofibrosis MYL005 MYELOF
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 Sarcoma MYL003
Myeloid/lymphoid Neoplasm Associated with Pdgfrb Rearrangement MYL065
Myeloma, Multiple MYL069 MM
Myelomeningocele MYL020
Myelopathy, Htlv-1-Associated MYL057 HAM
Myeloperoxidase Deficiency MYL013 MPOD
Myelophthisic Anemia MYL002
Myeloproliferative Disorder, Chronic, with Eosinophilia MYL067 MPE
Myeloproliferative Neoplasm MYL031 MPD
Myeloproliferative Syndrome, Transient MYL058 MST
Myeloproliferative/lymphoproliferative Neoplasms, Familial MYL064 MPLPF
Myh-9 Related Disease MYH015
Myh9 Related Thrombocytopenia MYH004
Myhre Syndrome MYH012 MYHRS
Myiasis MYS004
Myo5b-Related Progressive Familial Intrahepatic Cholestasis MY5001
Myoblastoma MYB001
Myocardial Infarction MYC007 MCI1
Myocardial Infarction 2 MYC058 MCI2
Myocardial Stunning MYC005
Myocarditis MYC008
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 of Lafora MYC079 EPM2
Myoclonic Epilepsy of Unverricht and Lundborg MYC080 EPM1
Myoclonic Epilepsy, Familial Infantile MYC083 FIME
Myoclonic Epilepsy, Juvenile 3 MYC085 EJM3
Myoclonic Epilepsy, Juvenile 4 MYC086 EJM4
Myoclonic-Astastic Epilepsy MYC069 MAE
Myoclonic-Atonic Epilepsy MYC071 MAE
Myoclonus MYC033
Myoclonus and Ataxia MYC078
Myoclonus Epilepsy MYC026
Myoclonus, Familial, 1 MYC089 MYOCL1
Myoclonus, Familial, 2 MYC090 MYOCL2
Myoclonus, Intractable, Neonatal MYC075 NEIMY
Myoepithelial Carcinoma MYP002
Myoepithelioma MYP001
Myofascial Pain Syndrome MYF002
Myofibrillar Myopathy MYF003
Myofibroma MYF001
Myofibromatosis, Infantile, 1 MYF007 IMF1
Myofibromatosis, Infantile, 2 MYF010 IMF2
Myoglobinuria MYG005
Myoglobinuria, Acute Recurrent, Autosomal Recessive MYG004 ARARM
Myoglobinuria, Recurrent MYG007 RM-MT
Myoma MYM001 MYOMA
Myopathic Intestinal Pseudoobstruction MYP066
Myopathy MYP004
Myopathy Due to Myoadenylate Deaminase Deficiency MYP071 MMDD
Myopathy of Extraocular Muscle MYP005
Myopathy with Deficiency of Iscu MYP009
Myopathy with Extrapyramidal Signs MYP086 MPXPS
Myopathy with Lactic Acidosis, Hereditary MYP097 HML
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset MYP093 EMARDD
Myopathy, Autosomal Recessive, with Rigid Spine and Distal Joint Contractures MYP152 MRRSDC
Myopathy, Centronuclear, 1 MYP123 CNM1
Myopathy, Centronuclear, 2 MYP131 CNM2
Myopathy, Centronuclear, 4 MYP098 CNM4
Myopathy, Centronuclear, 5 MYP148 CNM5
Myopathy, Centronuclear, 6, with Fiber-Type Disproportion MYP150 CNM6
Myopathy, Centronuclear, X-Linked MYP136 CNMX
Myopathy, Congenital MYP132
Myopathy, Congenital, Bailey-Bloch MYP151 MYPBB
Myopathy, Congenital, Compton-North MYP038 MYPCN
Myopathy, Congenital, with Fast-Twitch Fiber Atrophy MYP154 MYOFTA
Myopathy, Congenital, with Fiber-Type Disproportion MYP091 CFTD
Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked MYP039 CFTDX
Myopathy, Congenital, with Tremor MYP155 MYOTREM
Myopathy, Distal, 1 MYP125 MPD1
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, Distal, with Rimmed Vacuoles MYP120 DMRV
Myopathy, Isolated Mitochondrial, Autosomal Dominant MYP099 IMMD
Myopathy, Lactic Acidosis, and Sideroblastic Anemia MYP108
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 MYP021 MLASA1
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 MYP022 MLASA2
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 MYP107 MLASA3
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay MYP017 MPMCHD
Myopathy, Mitochondrial, and Ataxia MYP149 MMYAT
Myopathy, Myofibrillar, 1 MYP072 MFM1
Myopathy, Myofibrillar, 2 MYP082 MFM2
Myopathy, Myofibrillar, 3 MYP078 MFM3
Myopathy, Myofibrillar, 4 MYP080 MFM4
Myopathy, Myofibrillar, 5 MYP079 MFM5
Myopathy, Myofibrillar, 6 MYP081 MFM6
Myopathy, Myofibrillar, 7 MYP119 MFM7
Myopathy, Myofibrillar, 8 MYP118 MFM8
Myopathy, Myofibrillar, 9, with Early Respiratory Failure MYP153 MFM9
Myopathy, Myofibrillar, Fatal Infantile Hypertonic, Alpha-B Crystallin-Related MYP121 MFMFIH-CRYAB
Myopathy, Myosin Storage, Autosomal Dominant MYP105 MSMA
Myopathy, Myosin Storage, Autosomal Recessive MYP106 MSMB
Myopathy, Proximal, and Ophthalmoplegia MYP139 MYPOP
Myopathy, Scapulohumeroperoneal MYP114 SHPM
Myopathy, Spheroid Body MYP094 SBM
Myopathy, Tubular Aggregate, 1 MYP087 TAM1
Myopathy, Tubular Aggregate, 2 MYP088 TAM2
Myopathy, Vacuolar, with Casq1 Aggregates MYP104 VMCQA
Myopathy, X-Linked, with Excessive Autophagy MYP100 MEAX
Myopathy, X-Linked, with Postural Muscle Atrophy MYP056 XMPMA
Myopericytoma MYP064
Myopia MYP006
Myopia 1, X-Linked MYP137 MYP1
Myopia 10 MYP044 MYP10
Myopia 11, Autosomal Dominant MYP143 MYP11
Myopia 12, Autosomal Dominant MYP144 MYP12
Myopia 13, X-Linked MYP134 MYP13
Myopia 14 MYP069 MYP14
Myopia 15, Autosomal Dominant MYP146 MYP15
Myopia 16, Autosomal Dominant MYP145 MYP16
Myopia 17, Autosomal Dominant MYP140 MYP17
Myopia 18, Autosomal Recessive MYP133 MYP18
Myopia 19, Autosomal Dominant MYP147 MYP19
Myopia 2, Autosomal Dominant MYP127 MYP2
Myopia 20, Autosomal Dominant MYP084 MYP20
Myopia 21, Autosomal Dominant MYP070 MYP21
Myopia 22, Autosomal Dominant MYP075 MYP22
Myopia 23, Autosomal Recessive MYP074 MYP23
Myopia 24, Autosomal Dominant MYP090 MYP24
Myopia 25, Autosomal Dominant MYP117 MYP25
Myopia 26, X-Linked, Female-Limited MYP135 MYP26
Myopia 3, Autosomal Dominant MYP138 MYP3
Myopia 5, Autosomal Dominant MYP141 MYP5
Myopia 6 MYP018 MYP6
Myopia 7 MYP040 MYP7
Myopia 8 MYP041 MYP8
Myopia 9 MYP048 MYP9
Myopia, High, with Cataract and Vitreoretinal Degeneration MYP073 MCVD
Myosclerosis, Autosomal Recessive MYS016 MYOSAR
Myositis MYS005 IIM
Myositis Fibrosa MYS002
Myositis Ossificans MYS001
Myostatin-Related Muscle Hypertrophy MYS010 MSLHP
Myotonia MYT011
Myotonia Congenita MYT023
Myotonia Congenita, Autosomal Dominant MYT027 MCAD
Myotonia Congenita, Autosomal Recessive MYT029 MCAR
Myotonia, Potassium-Aggravated MYT030 MYOSCN4A
Myotonic Disease MYT003
Myotonic Dystrophy MYT002
Myotonic Dystrophy 1 MYT021 DM1
Myotonic Dystrophy 2 MYT020 DM2
Myotubular Myopathy with Abnormal Genital Development MYT025
Myringitis Bullosa Hemorrhagica MYR001
Myxedema MYX004
Myxofibrosarcoma MYX013
Myxoid Chondrosarcoma MYX008
Myxoid Leiomyosarcoma MYX006
Myxoid Liposarcoma MYX005 MXLIPO
Myxoid Liposarcoma of the Ovary MYX002
Myxoma, Intracardiac MYX012 INTMYX
Myxopapillary Ependymoma MYX001
Myxosarcoma MYX007
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