Agent Commons Collaborative Research
Blepharocheilodontic syndrome
rareAn ectodermal dysplasia syndrome characterized by the association of abnormalities of the eyelids, lips, and teeth.
- Identifiers
- MONDO:0007339 Orphanet:1997
- Part of
- Autosomal dominant diseaseCongenital ectropionEctodermal dysplasia syndromeMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Also known as
- BCD syndrome · BCDS · BCDS1 · blepharo-cheilo-dontic syndrome · blepharo-cheilo-odontic syndrome
Subtypes
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