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List of all diseases starting with M

• MAJEED SYNDROME; MJDS (LPIN2) MIM=609628
• MALEYLACETOACETATE ISOMERASE MIM=617596
• MALONYL-COA DECARBOXYLASE DEFICIENCY MIM=248360
• MAMEL (METHYLMALONIC ACIDURIA MITOCHONDRIAL ENCEPHELOPATHY LEIGH-LIKE) A NEW MITOCHONDRIAL ENCEPHALOPATHY MIM=
• MAPLE SYRUP URINE DISEASE (MSUD) MIM=248600
• MAPLE SYRUP URINE DISEASE, MILD VARIANT (MSUDMV) MIM=615135
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 1 (MODY1) MIM=125850
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10 (MODY10) MIM=613370
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11 (MODY11) MIM=613375
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13 (MODY13) MIM=616329
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14 (MODY14) MIM=616511
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 2 (MODY2) MIM=125851
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (MODY3) MIM=600496
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4 (MODY4) MIM=606392
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 5 (MODY5, RCAD) MIM=137920
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 (MODY6) MIM=606394
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7 (MODY7) MIM=610508
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, (MODY 8) WITH EXOCRINE DYSFUNCTION MIM=609812
• MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (MODY9) MIM=612225
• MAURIAC SYNDROME MIM=---
• MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY ? MIM=602199
• MEDIUM CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (MCAD) MIM=201450
• MEGALOBLASTIC ANEMIA 1 (IMERSLUND-GRASBECK SYNDROME, IGS) MIM=261100
• MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY (DHFRD) MIM=613839
• MENKES SYNDROME (MNK) MIM=309400
• MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD (MED13L) MIM=616789
• MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12 (CDG) MIM=611090
• MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14; MRT14 MIM=614020
• MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 (MAN1B1-CDG) MIM=614202
• MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7 (CDG) MIM=611093
• MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND MIM=609313
• MENTAL RETARDATION, X-LINKED 91; MRX91 MIM=300577
• MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR MIM=309583
• METABOLIC CRISES, RECURRENT, WITH VARIABLE ENCEPHALOMYOPATHIC FEATURES AND NEUROLOGIC REGRESSION (MECREN) MIM=618416
• METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION (MECR
• METACHROMATIC LEUKODISTROPHY (MLD) MIM=250100
• METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY MIM=249900
• METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA MIM=614875
• METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE MIM=250800
• METHEMOGLOBINEMIA TYPE IV MIM=250790
• METHIONINE ADENOSYLTRANSFERASE I/III DEFICIENCY (MAT, MAT1A) MIM=250850
• METHIONINE ADENOSYLTRANSFERASE II, ALPHA (MAT2A) MIM=601468
• METHIONINE MALABSORPTION MIM=250900
• METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY (MMSDH) MIM=614105
• METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE MIM=309541
• METHYLMALONIC ACIDURIA (MMA) MIM=251000
• METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO ZNF143 DEFICIENCY MIM=603433
• METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE MIM=277400
• METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblD TYPE MIM=277410
• METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE MIM=614857
• METHYLMALONIC ACIDURIA, ATYPICAL MIM=
• METHYLMALONIC ACIDURIA, cblA TYPE MIM=251100
• METHYLMALONIC ACIDURIA, cblB TYPE MIM=251110
• METHYLMALONIC ACIDURIA, ISOLATED, BENIGN (BACTERIAL OVERGROWTH?) MIM=
• METHYLMALONIC ACIDURIA, TRANSIENT, DUE TO TRANSCOBALAMIN RECEPTOR DEFECT MIM=613646
• METHYLMALONYL-CoA EPIMERASE DEFICIENCY (MCEE) MIM=251120
• MEVALONIC ACIDURIA (MKD) MIM=610377
• MICROPHTHALMIA, SYNDROMIC 9 (MCOPS9) MIM=601186
• MITCHELL-RILEY SYNDROME (MTCHRS) MIM=615710
• MITOCHONDRIAL ASPARTATE AMINOTRANSFERASE DEFICIENCY MIM=138150
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1 (MC1DN1) MIM=252010
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10 (MC1DN10) MIM=618233
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11 (MC1DN11) MIM=618234
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12 (MC1DN12) MIM=301020
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13 (MC1DN13) MIM=618235
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14 (MC1DN14) MIM=618236
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15 (MC1DN15) MIM=618237
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16 (MC1DN16) MIM=618238
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17 (MC1DN17) MIM=618239
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18 (MC1DN18) MIM=618240
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19 (MC1DN19) MIM=618241
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2 (MC1DN2) MIM=618222
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20 (MC1DN20, ACAD9) MIM=611126
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21 (MC1DN21) MIM=618242
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22 (MC1DN22) MIM=618243
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23 (MC1DN23) MIM=618244
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24 (MC1DN24) MIM=618245
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25 (MC1DN25) MIM=618246
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26 (MC1DN26) MIM=618247
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27 (MC1DN27) MIM=618248
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28 MIM=618249
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29 (MC1DN29) MIM=618250
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31 (MC1DN31) MIM=618251
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32 (MC1DN32) MIM=618252
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33 (MC1DN33) MIM=618253
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34; MC1DN34 MIM=618776
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3 MIM=618224
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4 (MC1DN4) MIM=618225
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5 (MC1DN5) MIM=618226
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6 (MC1DN6) MIM=618228
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7 (MC1DN7) MIM=618229
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8 (MC1DN8) MIM=618230
• MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9 (MC1DN9) MIM=618232
• MITOCHONDRIAL COMPLEX II DEFICIENCY MIM=252011
• MITOCHONDRIAL COMPLEX III DEFICIENCY MIM=124000
• MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4 (MC3DN4) MIM=615159
• MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 (MC3DN6) MIM=615453
• MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 (MC3DN7) MIM=615824
• MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9 (MC3DN9) MIM=616111
• MITOCHONDRIAL COMPLEX IV DEFICIENCY MIM=220110
• MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY MIM=604273
• MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2 MIM=614052
• MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3 (MC5DN3) MIM=614053
• MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 (MC5DN4) MIM=615228
• MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5 MIM=618120
• MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE) MIM=603041
• MITOCHONDRIAL DNA DEPLETION SYNDROME 11; MTDPS11 MIM=615084
• MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A MIM=617184
• MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE; MTDPS12B MIM=615418
• MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE); MTDPS13 MIM=615471
• MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE); MTDPS14 MIM=616896
• MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15 MIM=617156
• MITOCHONDRIAL DNA DEPLETION SYNDROME 16 (HEPATIC TYPE) (MTDPS16) MIM=618528
• MITOCHONDRIAL DNA DEPLETION SYNDROME 17 (MTDPS17) MIM=618567
• MITOCHONDRIAL DNA DEPLETION SYNDROME 18 (MTDPS18) MIM=618811
• MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MTDPS2) MIM=609560
• MITOCHONDRIAL DNA DEPLETION SYNDROME 3 MIM=251880
• MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) MIM=203700
• MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B MIM=613662
• MITOCHONDRIAL DNA DEPLETION SYNDROME 5 MIM=612073
• MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE); MTDPS6 MIM=256810
• MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE); MTDPS7 MIM=271245
• MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (MNGIE) MIM=612075
• MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA); MTDPS9; SUCGL1 MIM=245400
• MITOCHONDRIAL MYOPATHY WITH DIABETES MIM=500002
• MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS (MMLA) MIM=251950
• MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OR WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY (MEOAL) MIM=251900
• MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY MIM=610773
• MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY (MPYCD) MIM=614741
• MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY (ECHS1D, SCEH) MIM=616277
• MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY (MTPD, HADHA) MIM=609015
• MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY (MTPD, HADHB) MIM=609015
• MITOCHONDRIAL tRNA(Phe) DEFICIENCY (MT-TF) MIM=???
• MITOCHONDRIAL-ENCEPHALOPATHY-LACTIC ACIDOSIS-STROKE (MELAS) MIM=540000
• MOHR-TRANEBJAERG SYNDROME; MTS MIM=304700
• MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A (MOCODA) MIM=252150
• MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B (MOCODB) MIM=252160
• MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C (MOCODC) MIM=615501
• MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY MIM=616095
• MORFAN SYNDROME MIM=---
• MUCOLIPIDOSIS II MIM=252500
• MUCOLIPIDOSIS III ALPHA/BETA MIM=252600
• MUCOLIPIDOSIS III GAMMA MIM=252605
• MUCOLIPIDOSIS IV MIM=252650
• MUCOPOLYSACCHARIDOSIS I-H; HURLER SYNDROME (MPS1-H) MIM=607014
• MUCOPOLYSACCHARIDOSIS I-S; SCHEIE SYNDROME MIM=607016
• MUCOPOLYSACCHARIDOSIS II; HUNTER SYNDROME MIM=309900
• MUCOPOLYSACCHARIDOSIS III; SAN FILIPPO A SYNDROME MIM=252900
• MUCOPOLYSACCHARIDOSIS III; SAN FILIPPO B SYNDROME MIM=252920
• MUCOPOLYSACCHARIDOSIS III; SAN FILIPPO C SYNDROME MIM=252930
• MUCOPOLYSACCHARIDOSIS III; SAN FILIPPO D SYNDROME MIM=252940
• MUCOPOLYSACCHARIDOSIS IV; MORQUIO A SYNDROME MIM=253000
• MUCOPOLYSACCHARIDOSIS IV; MORQUIO B SYNDROME MIM=253010
• MUCOPOLYSACCHARIDOSIS IX MIM=601492
• MUCOPOLYSACCHARIDOSIS TYPE IH/S; HURLER-SCHEIE SYNDROME MIM=607015
• MUCOPOLYSACCHARIDOSIS VI; MAROTEAUX-LAMY SYNDROME MIM=253200
• MUCOPOLYSACCHARIDOSIS VII; SLY SYNDROME MIM=253220
• MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME (MPSPS) MIM=617303
• MULTIPLE CARBOXYLASE DEFICIENCY, NEONATAL OR EARLY ONSET FORM (HLCS) MIM=253270
• MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3 (MCAHS3) MIM=615398
• MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 (MMDS1) MIM=605711
• MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA (MMDS2) MIM=614299
• MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3 (MMDS3) MIM=615330
• MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4 (MMDS4) MIM=616370
• MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5 (MMDS5) MIM=617613
• MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6 (MMDS6) MIM=617954
• MULTIPLE SULFATASE DEFICIENCY (MSD) MIM=272200
• MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY (MDCCAID, INPP5K)) MIM=617404
• MYOADENYLATE DEAMINASE DEFICIENCY (AMPDA) MIM=615511
• MYOCLONIC EPILEPSY AND RAGGED RED FIBER DISEASE (MERRF) MIM=545000
• MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE (LPIN1) MIM=268200
• MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT MIM=256960
• MYOPATHY OR CARDIOMYOPATHY DUE TO DESMIN DEFECT MIM=601419
• MYOPATHY WITH LACTIC ACIDOSIS, HEREDITARY (HML, ISCU) MIM=255125
• MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1 (MLASA1) MIM=600462
• MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2 (MLASA2) MIM=613561
• MYOPATHY, MITOCHONDRIAL, AND ATAXIA (MMYAT) MIM=617675