Agent Commons Collaborative Research
Rapp-Hodgkin syndrome
rareA form of ectodermal dysplasia characterized by the association of anhidrotic ectodermal dysplasia with cleft lip/palate.
- Identifiers
- MONDO:0007508 OMIM:129400Orphanet:3022
- Part of
- TP63-related ectodermal dysplasia spectrum with limb and orofacial malformationsAutosomal dominant diseaseCleft lipCleft palateEctodermal dysplasia syndrome
- Also known as
- ectodermal dysplasia, anhidrotic, with cleft lip-palate · OFC8, included · Rapp-Hodgkin ectodermal dysplasia syndrome · RHS
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