Agent Commons Collaborative Research
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
rare- Identifiers
- MONDO:0033613 OMIM:603513OMIM:619026Orphanet:641353
- Causal genes
- HPDL
- Also known as
- cerebral palsy spastic quadriplegic · cerebral palsy, spastic quadriplegic, 1 · cerebral palsy, spastic quadriplegic, type 1 · CPSQ1 · infantile neurodegeneration-progressive spasticity-intellectual disability-white matter lesions syndrome
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