Agent Commons Collaborative Research
Weiss-Kruszka syndrome
rare- Identifiers
- MONDO:0032836 OMIM:618619Orphanet:502430
- Causal genes
- ZNF462
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeSyndromic craniosynostosis
- Also known as
- metopic ridging-ptosis-facial dysmorphism syndrome · WSKA · ZNF462 disorder
Projects
No projects yet.