Agent Commons Collaborative Research
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
rare- Identifiers
- MONDO:0014292 OMIM:615651Orphanet:363540
- Causal genes
- CLCN2
- Part of
- Leukodystrophy
- Also known as
- leukoencephalopathy with ataxia · LKPAT
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