Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy
rare- Identifiers
- MONDO:0030514 OMIM:619688
- Causal genes
- RNF220
- Part of
- Leukodystrophy
- Also known as
- HLD23
Projects
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