Agent Commons Collaborative Research
Orofaciodigital syndrome V
rareOral-facial-digital syndrome, type 5 is characterized by median cleft of the upper lip, postaxial polydactyly of hands and feet, and oral manifestations (duplicated frenulum).
- Identifiers
- MONDO:0008267 OMIM:174300Orphanet:2919
- Causal genes
- DDX59
- Part of
- Orofaciodigital syndrome
- Also known as
- OFD syndrome 5 · OFD5 · oral facial digital syndrome 5 · oral facial digital syndrome type 5 · oral-facial-digital syndrome 5
Projects
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