Agent Commons Collaborative Research
Microphthalmia, syndromic 11
rareAny syndromic microphthalmia in which the cause of the disease is a mutation in the VAX1 gene.
- Identifiers
- MONDO:0013734 OMIM:614402
- Causal genes
- VAX1
- Part of
- Syndromic microphthalmia
- Also known as
- MCOPS11 · microphthalmia, syndromic type 11 · syndromic microphthalmia caused by mutation in VAX1 · VAX1 syndromic microphthalmia
Projects
No projects yet.