A–Z DIRECTORY
Conditions beginning with C
- Congenital bile acid synthesis defect type 2Autosomal recessive
- Congenital cataracts, facial dysmorphism, and neuropathyAutosomal recessive
- Congenital central hypoventilation syndromeAutosomal dominant
- Congenital contractural arachnodactylyAutosomal dominant
- Congenital deafness with labyrinthine aplasia, microtia, and microdontiaAutosomal recessive
- Congenital diaphragmatic herniaPattern unknown
- Congenital dyserythropoietic anemiaAutosomal recessive · Autosomal dominant, inherited from one affected parent
- Congenital fiber-type disproportionAutosomal recessive · Autosomal dominant · X-linked
- Congenital fibrosis of the extraocular musclesAutosomal recessive · Autosomal dominant
- Congenital generalized lipodystrophyAutosomal recessive
- Congenital hepatic fibrosisAutosomal dominant · X-linked recessive · Autosomal recessive
- Congenital hyperinsulinismAutosomal dominant · Autosomal recessive
- Congenital hypothyroidismAutosomal dominant · Autosomal recessive
- Congenital insensitivity to pain with anhidrosisAutosomal recessive
- Congenital leptin deficiencyAutosomal recessive
- Congenital mirror movement disorderAutosomal recessive · Autosomal dominant, inherited from one affected parent
- Congenital myasthenic syndromesAutosomal recessive · Autosomal dominant
- Congenital nephrotic syndromeAutosomal recessive
- Congenital plasminogen deficiencyAutosomal recessive
- Congenital stromal corneal dystrophyAutosomal dominant, or a new variant
- Congenital sucrase-isomaltase deficiencyAutosomal recessive
- Constitutional mismatch repair deficiency syndromeAutosomal recessive · Autosomal dominant
- Core binding factor acute myeloid leukemiaNot inherited
- Cornelia de Lange syndromeX-linked recessive · Autosomal dominant
- Corticosteroid-binding globulin deficiencyAutosomal recessive
- Corticosterone methyloxidase deficiencyAutosomal recessive
- Costeff syndromeAutosomal recessive
- Costello syndromeAutosomal dominant, or a new variant
- Cowden syndromeAutosomal dominant
- Cranioectodermal dysplasiaAutosomal recessive
- Craniofacial microsomiaAutosomal dominant · Autosomal recessive
- Craniofacial-deafness-hand syndromeAutosomal dominant
- Craniofrontonasal syndromeX-linked
- Craniometaphyseal dysplasiaAutosomal recessive · Autosomal dominant
- Cri-du-chat syndromeNot inherited
- Crigler-Najjar syndromeAutosomal recessive
- Critical congenital heart diseasePattern unknown
- Crohn's diseasePattern unknown
- Crouzon syndromeAutosomal dominant
- Crouzon syndrome with acanthosis nigricansAutosomal dominant
- Cryopyrin-associated periodic syndromes
- Cryptogenic cirrhosisAutosomal dominant · Not inherited · Pattern unknown
- CUL3-related neurodevelopmental disorderAutosomal dominant, or a new variant
- Cushing diseasePattern unknown
- Cutis laxaAutosomal recessive · X-linked recessive · Autosomal dominant
- Cyclic neutropeniaAutosomal dominant
- Cyclic vomiting syndromeMitochondrial · Pattern unknown
- CYLD cutaneous syndrome
- Cystic fibrosisAutosomal recessive
- CystinosisAutosomal recessive
- CystinuriaAutosomal recessive
- Cytochrome c oxidase deficiencyMitochondrial · Autosomal recessive
- Cytochrome P450 oxidoreductase deficiencyAutosomal recessive
- Cytogenetically normal acute myeloid leukemiaAutosomal dominant · Not inherited
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