back 1 2 3 5 A B C D E F G H I J K L M N O P R S T U V W X Y Z

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List of all diseases starting with C

• CALFAN SYNDROME MIM=616719
• CANAVAN DISEASE (ASPA) MIM=271900
• CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY (CPS) MIM=237300
• CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO; CA5AD MIM=615751
• CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3 (CEMCOX3) MIM=616500
• CARDIOMYOPATHY, FAMILIAL DILATED MIM=115200
• CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (CMH6) MIM=600858
• CARNITINE DEFICIENCY, MYOPATHIC MIM=212160
• CARNITINE PALMITOYL TRANSFERASE DEFICIENCY (I); CPT1 MIM=255120
• CARNITINE PALMITOYL TRANSFERASE DEFICIENCY (II), CPT2, LETHAL NEONATAL MIM=608836
• CARNITINE PALMITOYL TRANSFERASE DEFICIENCY (II), CPT2, MYOPATHIC, STRESS-INDUCED MIM=255110
• CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, CPT2, INFANTILE MIM=600649
• CARNITINE TRANSPORTER DEFICIENCY; PRIMARY SYSTEMIC CARNITINE DEFICIENCY MIM=212140
• CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY (CACT) MIM=212138
• CARNOSINURIA, CARNOSINEMIA MIM=212200
• CATARACT 47 (CTRCT47) MIM=612018
• CATIONIC AMINO ACID TRANSPORTER 2 (CAT-2) DEFECT MIM=601872
• CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS (CAPOS) [DD] MIM=601338
• CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1; CREATINE-TRANSPORTER DEFECT (CTD) MIM=300352
• CEREBRAL CREATINE DEFICIENCY SYNDROME 2; CCDS2; GAMT DEFICIENCY MIM=612736
• CEREBRAL CREATINE DEFICIENCY SYNDROME 3 (GAMT, AGAT DEFICIENCY) MIM=612718
• CEREBRAL FOLATE DEFICIENCY DUE TO FOLR1 AUTOANTIBODIES (CFD) MIM=---
• CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 1 (CPSQ1) MIM=603513
• CEROID LIPOFUSCINOSIS, NEURONAL, 1 (SANTAVUORI-HALTIA-DISEASE) MIM=256730
• CEROID LIPOFUSCINOSIS, NEURONAL, 10 MIM=610127
• CEROID LIPOFUSCINOSIS, NEURONAL, 11 MIM=614706
• CEROID LIPOFUSCINOSIS, NEURONAL, 12 MIM=606693
• CEROID LIPOFUSCINOSIS, NEURONAL, 13 MIM=615362
• CEROID LIPOFUSCINOSIS, NEURONAL, 14 MIM=611726
• CEROID LIPOFUSCINOSIS, NEURONAL, 2 MIM=204500
• CEROID LIPOFUSCINOSIS, NEURONAL, 3 (CLN3) MIM=204200
• CEROID LIPOFUSCINOSIS, NEURONAL, 4A MIM=204300
• CEROID LIPOFUSCINOSIS, NEURONAL, 4B MIM=162350
• CEROID LIPOFUSCINOSIS, NEURONAL, 5 MIM=256731
• CEROID LIPOFUSCINOSIS, NEURONAL, 6 MIM=601780
• CEROID LIPOFUSCINOSIS, NEURONAL, 7 MIM=610951
• CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT MIM=610003
• CEROID LIPOFUSCINOSIS, NEURONAL, 8; CLN8 MIM=600143
• CEROID LIPOFUSCINOSIS, NEURONAL, 9 MIM=609055
• CHILD SYNDROME MIM=308050
• CHILDHOOD CNS TUMORS [DD] MIM=
• CHILDHOOD VASCULITIS [DD] MIM=611775
• CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 1; PFIC1 MIM=211600
• CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 2 (PFIC2) MIM=601847
• CHOLESTATIC LIVER DISEASE [DD] MIM=---
• CHOLESTERYL ESTER STORAGE DISEASE MIM=278000
• CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT MIM=118650
• CHONDRODYSPLASIA PUNCTATA, X-LINKED RECESSIVE MIM=302950
• CHONDRODYSPLASIA PUNCTATA2, X-LINKED DOMINANT MIM=302960
• CHONDRODYSTROPHIA CALCIFICANS CONGENITA MIM=215100
• CHRONIC DIARRHEA [DD] MIM=
• CITRULLINEMIA TYPE I (ASS) MIM=215700
• CITRULLINEMIA TYPE II, ADULT-ONSET MIM=603471
• CITRULLINEMIA TYPE II, NEONATAL ONSET (NICCD) MIM=605814
• CK SYNDROME MIM=300831
• CLATHRIN (CTLC) VARIATION MIM=617854
• COBALAMIN F DISEASE (cblF) MIM=277380
• COBALAMIN MALABSORPTION MIM=
• COENZYME Q10 DEFICIENCY, PRIMARY, 1 (COQ10D1) MIM=607426
• COENZYME Q10 DEFICIENCY, PRIMARY, 2 (COQ10D2) MIM=614651
• COENZYME Q10 DEFICIENCY, PRIMARY, 3 (COQ10D3) MIM=614652
• COENZYME Q10 DEFICIENCY, PRIMARY, 4 (COQ10D4) MIM=612016
• COENZYME Q10 DEFICIENCY, PRIMARY, 5 (COQ10D5) MIM=614654
• COENZYME Q10 DEFICIENCY, PRIMARY, 6 (COQ10D6) MIM=614650
• COENZYME Q10 DEFICIENCY, PRIMARY, 7 (COQ10D7) MIM=616276
• COENZYME Q10 DEFICIENCY, PRIMARY, 8 (COQ10D8) MIM=616733
• COENZYME Q10 DEFICIENCY, PRIMARY, ? (COQ10D?) MIM=616359
• COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA (CIMAH) MIM=617780
• COMBINED MALONIC AND METHYLMALONIC ACIDURIA (CHAMMA) MIM=614265
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1 (COXPD1) MIM=609060
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10; COXPD10 (MTO1) MIM=614702
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11 MIM=614922
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12 MIM=614924
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13 MIM=614932
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14 MIM=614946
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15 MIM=614947
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16 MIM=615395
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17; COXPD17 MIM=615440
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18; COXPD18 MIM=615578
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19 (COXPD19) MIM=615595
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20 (COXPD20) MIM=615917
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21; COXPD21 MIM=615918
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22; COXPD22 MIM=616045
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23; COXPD23 MIM=616198
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24 MIM=616239
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25 MIM=616430
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26 MIM=616539
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27 MIM=616672
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28; COXPD28 MIM=616794
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29; COXPD29 MIM=616811
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2 MIM=610498
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30; COXPD30 MIM=616974
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31; COXPD31 MIM=617228
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32 MIM=617664
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33 MIM=617713
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34 MIM=617872
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35 MIM=617873
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36 MIM=617950
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 37; COXPD37 MIM=618329
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38; COXPD38 MIM=613878
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 39; COXPD39 MIM=618397
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3; COXPD3 MIM=610505
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40 (COXPD40) MIM=618835
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41 (COXPD41) MIM=618838
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42 (COXPD42) MIM=618839
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43 (COXPD43) MIM=618851
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44 (COXPD44) MIM=618855
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45 (COXPD45) MIM=618951
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46 (COXPD46) MIM=618952
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47 (COXPD47) MIM=618958
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48 (COXPD48) MIM=619012
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4 MIM=610678
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5; COXPD5 MIM=611719
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6 MIM=300816
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7 MIM=613559
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8 MIM=614096
• COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9 MIM=614582
• COMBINED SAPOSIN DEFICIENCY MIM=611721
• CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION (CHLND) MIM=614482
• CONGENITAL CHLORIDE DIARRHEA MIM=214700
• CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG (NGLY1-CDDG) MIM=615273
• CONGENITAL DISORDER OF GLYCOSYLATION MIM=
• CONGENITAL DISORDER OF GLYCOSYLATION (CSGALNACT1) MIM=616615
• CONGENITAL DISORDER OF GLYCOSYLATION (TSTA3) MIM=---
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ia (PMM2-CDG) MIM=212065
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ib (MPI) MIM=602579
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ic MIM=603147
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Id MIM=601110
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ie MIM=608799
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-If MIM=609180
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ig MIM=607143
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ih MIM=608104
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ii MIM=607906
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIa MIM=212066
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIb MIM=606056
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIc MIM=266265
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IId MIM=607091
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIe MIM=608779
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIf MIM=603585
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIg MIM=611209
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIh MIM=611182
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIj MIM=613489
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIk MIM=614727
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIL MIM=614576
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIm (SLC35A2-CDG) MIM=300896
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIn MIM=616721
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIo MIM=616828
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-IIp MIM=616829
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ij MIM=608093
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ik MIM=608540
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Il MIM=608776
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Im MIM=610768
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-In MIM=612015
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Io MIM=612937
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ip MIM=613661
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ir MIM=614507
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Is MIM=300884
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-It MIM=614921
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Iu MIM=615042
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Iw MIM=615596
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Ix MIM=615597
• CONGENITAL DISORDER OF GLYCOSYLATION CDG-Iy MIM=300934
• CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION (CDGF) MIM=618005
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa; CDG1AA MIM=617082
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Icc; CDG-ICC MIM=301031
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG-IIi MIM=613612
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q MIM=617395
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIr (CDG2R) MIM=301045
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIt (CDG2T) MIM=618885
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq;CDG-Iq MIM=612379
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu MIM=615042
• CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw MIM=615596
• CONGENITAL ERYTHTOPOIETIC PORPHYRIA (CEP, GUNTHER DISEASE) MIM=263700
• CONGENITAL GLUTAMINE DEFICIENCY; GLUTAMINE SYNTHASE DEFICIENCY MIM=610015
• CONGENITAL HYPERINSULINISM AND HYPOPITUITARISM (NEW DISEASE?) MIM=600288
• CONGENITAL SECRETORY DIARRHOEA MIM=270420
• COPPER CHAPERONE FOR SUPEROXIDE DISMUTASE (CCS) MIM=603864
• COPROPORPHYRIA, HEREDITARY (HCP) MIM=121300
• CORTICOSTERONE METHYL OXIDASE I DEFICIENCY- CMO I MIM=203400
• CORTICOSTERONE METHYL OXIDASE II DEFICIENCY - CMO II MIM=610600
• CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2 MIM=614662
• COSMETICS, VITAMINES, DRUGS AND DRUG METABOLITES [DD] MIM=
• CRIGLER-NAJJAR SYNDROME TYPE I MIM=218800
• CRIGLER-NAJJAR SYNDROME TYPE II MIM=606785
• CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA, WITH CONGENITAL DISORDER OF GLYCOSYLATION; ARCL2A (CDG) MIM=219200
• CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB; ARCL2B MIM=612940
• CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA; ARCL3A MIM=219150
• CYCLIC VOMITING SYNDROME (CSV) MIM=500007
• CYSTATHIONINURIA MIM=219500
• CYSTIC FIBROSIS (CF) MIM=219700
• CYSTINE-LYSINURIA MIM=222350
• CYSTINOSIS, ADULT NONNEPHROPATHIC MIM=219750
• CYSTINOSIS, INFANTILE NEPHROPATHIC (CTNS) MIM=219800
• CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE MIM=219900
• CYSTINURIA MIM=220100
• CYSTINYLGLYCINURIA MIM=179780
• CYTOCHROME b OF COMPLEX III; MTCYB MIM=516020