Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 9
rareAny leukodystrophy in which the cause of the disease is a mutation in the RARS gene.
- Identifiers
- MONDO:0014506 OMIM:616140Orphanet:438114
- Causal genes
- RARS1
- Part of
- Leukodystrophy
- Also known as
- HLD9 · hypomyelinating leukodystrophy 9 · hypomyelinating leukodystrophy type 9 · leukodystrophy caused by mutation in RARS · leukodystrophy, hypomyelinating, type 9
Projects
No projects yet.