A–Z DIRECTORY
Conditions beginning with C
- C3 glomerulopathyAutosomal recessive
- Caffey diseaseAutosomal dominant
- Campomelic dysplasiaAutosomal dominant
- Camurati-Engelmann diseaseAutosomal dominant
- Canavan diseaseAutosomal recessive
- Cantú syndromeAutosomal dominant
- Cap myopathyNot inherited · Autosomal dominant
- Capillary malformation-arteriovenous malformation syndromeAutosomal dominant
- Carbamoyl phosphate synthetase I deficiencyAutosomal recessive
- Carbonic anhydrase VA deficiencyAutosomal recessive
- Cardiofaciocutaneous syndromeAutosomal dominant
- Carney complexAutosomal dominant, or a new variant
- Carnitine palmitoyltransferase I deficiencyAutosomal recessive
- Carnitine palmitoyltransferase II deficiencyAutosomal recessive
- Carnitine-acylcarnitine translocase deficiencyAutosomal recessive
- Carpal tunnel syndromePattern unknown
- Carpenter syndromeAutosomal recessive
- Cartilage-hair hypoplasiaAutosomal recessive
- CASK-related intellectual disabilityX-linked dominant
- Catecholaminergic polymorphic ventricular tachycardiaAutosomal dominant · Autosomal recessive
- CATSPER1-related nonsyndromic male infertilityAutosomal recessive
- Caudal regression syndromePattern unknown
- CAV3-related distal myopathyAutosomal dominant
- CDKL5 deficiency disorderX-linked dominant
- Celiac diseasePattern unknown
- Central core diseaseAutosomal recessive · Autosomal dominant
- Central precocious pubertyAutosomal dominant
- Centronuclear myopathyAutosomal dominant · Autosomal recessive
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyAutosomal dominant
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathyAutosomal recessive
- Cerebral cavernous malformationAutosomal dominant
- Cerebral folate transport deficiencyAutosomal recessive
- Cerebro-facio-thoracic dysplasiaAutosomal recessive
- Cerebrotendinous xanthomatosisAutosomal recessive
- Chanarin-Dorfman syndromeAutosomal recessive
- Channelopathy-associated congenital insensitivity to painAutosomal recessive
- Char syndromeAutosomal dominant
- Charcot-Marie-Tooth diseaseAutosomal dominant · X-linked dominant · Autosomal recessive
- CHARGE syndromeAutosomal dominant
- CHD2 myoclonic encephalopathyAutosomal dominant
- Chediak-Higashi syndromeAutosomal recessive
- CherubismAutosomal dominant
- CHILD syndromeX-linked dominant
- Childhood absence epilepsyAutosomal dominant
- Childhood myocerebrohepatopathy spectrumAutosomal recessive
- CHMP2B-related frontotemporal dementiaAutosomal dominant
- CholangiocarcinomaPattern unknown · Not inherited
- CHOPS syndromeAutosomal dominant
- ChordomaAutosomal dominant · Not inherited
- Chorea-acanthocytosisAutosomal recessive
- ChoroideremiaX-linked recessive
- Christianson syndromeX-linked recessive
- Chronic atrial and intestinal dysrhythmiaAutosomal recessive
- Chronic granulomatous diseaseAutosomal recessive · X-linked recessive
- Chronic myeloid leukemiaNot inherited
- CHST3-related skeletal dysplasiaAutosomal recessive
- Chylomicron retention diseaseAutosomal recessive
- CitrullinemiaAutosomal recessive
- CLCN2-related leukoencephalopathyAutosomal recessive
- Cleidocranial dysplasiaAutosomal dominant
- CLN1 diseaseAutosomal recessive
- CLN10 diseaseAutosomal recessive
- CLN11 diseaseAutosomal recessive
- CLN2 diseaseAutosomal recessive
- CLN3 diseaseAutosomal recessive
- CLN4 diseaseAutosomal dominant
- CLN5 diseaseAutosomal recessive
- CLN6 diseaseAutosomal recessive
- CLN7 diseaseAutosomal recessive
- CLN8 diseaseAutosomal recessive
- Clopidogrel resistanceAutosomal codominant
- Clouston syndromeAutosomal dominant
- CLPB deficiencyAutosomal recessive
- Coats plus syndromeAutosomal recessive
- Cockayne syndromeAutosomal recessive
- Coffin-Lowry syndromeX-linked dominant
- Coffin-Siris syndromeAutosomal dominant
- COG5-congenital disorder of glycosylationAutosomal recessive
- Cohen syndromeAutosomal recessive
- COL4A1-related brain small-vessel diseaseAutosomal dominant
- Cold-induced sweating syndromeAutosomal recessive
- Cole diseaseAutosomal dominant
- Collagen VI-related dystrophyAutosomal dominant · Autosomal recessive
- ColobomaX-linked recessive · X-linked dominant · Autosomal recessive · Not inherited · Autosomal dominant
- Color vision deficiencyX-linked recessive · Autosomal dominant
- Combined malonic and methylmalonic aciduriaAutosomal recessive
- Combined oxidative phosphorylation deficiency 1Autosomal recessive
- Combined pituitary hormone deficiencyAutosomal recessive · X-linked · Autosomal dominant, or a new variant
- Common variable immune deficiencyAutosomal recessive · Autosomal dominant · Pattern unknown
- Complement component 2 deficiencyAutosomal recessive
- Complement component 8 deficiencyAutosomal recessive
- Complement factor I deficiencyAutosomal recessive
- Complete LCAT deficiencyAutosomal recessive
- Complete plasminogen activator inhibitor 1 deficiencyAutosomal recessive
- Cone-rod dystrophyAutosomal dominant · X-linked recessive · Autosomal recessive
- Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiencyAutosomal recessive
- Congenital afibrinogenemiaAutosomal recessive
- Congenital anomalies of kidney and urinary tractPattern unknown · Autosomal recessive · Not inherited · Autosomal dominant
- Congenital bilateral absence of the vas deferensAutosomal recessive
- Congenital bile acid synthesis defect type 1Autosomal recessive
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