Disease list (C)
C1q deficiencyC7 deficiency
Camurati-Engelmann disease
Candidiasis, familial, 2, autosomal recessive (CARD9 deficiency)
Carnitine palmitoyltransferase II deficiency, lethal neonatal
Cartilage-hair hypoplasia
Cataract Congenital Cerulean, Type 3
Cerebral palsy, spastic quadriplegic, 3, formerly
cerebrotendinous xanthomatosis
Ceroid lipofuscinosis, neuronal, 3
Ceroid lipofuscinosis, neuronal, 6
Chanarin-Dorfman Syndrome
Charcot-Marie-Tooth Disease Type 4A
Charcot-Marie-Tooth Disease Type 4B2
Charcot-Marie-Tooth Disease Type 4C
Charcot-Marie-Tooth Disease, Axonal, Type 2B
Charcot-Marie-Tooth Disease, Axonal, Type 2B1
Charcot-Marie-Tooth neuropathy, X-linked dominant, 1
CHARGE syndrome
Chromosome 15q11-q13 duplication Syndrome
Chromosome 17q21.31 duplication syndrome
Chronic granulomatous disease due to deficiency of NCF-1
Chronic granulomatous disease due to deficiency of NCF-2
Chronic granulomatous disease, X-linked
Chronic mucocutaneous candidiasis disease
Chylomicron retention disease
Coenzyme Q10 deficiency, primary, 2
Colorectal cancer
Complement C4a defiency
Cone-rod dystrophy 18
Cone-Rode Dystrophy 3
Congenital Adrenal Hyperplasia, due to 21-Hydroxylase
Congenital disorder of glycosylation, Type IIe
Congenital disorder of glycosylation, type IIl
Congenital ichthyosis
Costello syndrome
Creutzfeldt-Jakob disease
Crigler-Najjar syndrome, type I
Cryptorchidism
Cystic fibrosis