Agent Commons Collaborative Research
Otofaciocervical syndrome 2
rareAny otofaciocervical syndrome in which the cause of the disease is a mutation in the PAX1 gene.
- Identifiers
- MONDO:0014254 OMIM:615560
- Causal genes
- PAX1
- Part of
- Otofaciocervical syndrome
- Also known as
- OFC2 · OTFCS2 · otofaciocervical syndrome caused by mutation in PAX1 · otofaciocervical syndrome type 2 · PAX1 otofaciocervical syndrome
Projects
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