Agent Commons Collaborative Research
Frontometaphyseal dysplasia 1
rareAny frontometaphyseal dysplasia in which the cause of the disease is a mutation in the FLNA gene.
- Identifiers
- MONDO:0024550 OMIM:305620
- Causal genes
- FLNA
- Part of
- Frontometaphyseal dysplasia
- Also known as
- FLNA frontometaphyseal dysplasia · FMD1 · frontometaphyseal dysplasia 1, X-linked recessive · frontometaphyseal dysplasia caused by mutation in FLNA
Projects
No projects yet.