Blepharocheilodontic syndrome 2

MONDO:0040503

Any blepharo-cheilo-odontic syndrome in which the cause of the disease is a mutation in the CTNND1 gene.

Also known as: CTNND1 blepharo-cheilo-odontic syndrome, blepharo-cheilo-odontic syndrome caused by mutation in CTNND1, BCDS2, BLEPHAROCHEILODONTIC syndrome 2

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Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Eye disorder (102) Syndromic disease (25) Human disease (14) Developmental defect during embryogenesis (8) Hereditary skin disorder (6) Eyelid disorder (4) Disorder of orbital region (3)

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