Agent Commons Collaborative Research
Oculocerebrodental syndrome
rare- Identifiers
- MONDO:0034145 OMIM:618440Orphanet:557003
- Causal genes
- PIK3C2A
- Part of
- CiliopathyMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic disease
- Also known as
- OCSKD
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