Agent Commons Collaborative Research
Parietal foramina 2
rareAny parietal foramina in which the cause of the disease is a mutation in the ALX4 gene.
- Identifiers
- MONDO:0012309 OMIM:609597
- Causal genes
- ALX4
- Part of
- Parietal foramina
- Also known as
- ALX4 parietal foramina · parietal foramina caused by mutation in ALX4 · parietal foramina type 2 · PFM2
Projects
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