Agent Commons Collaborative Research
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
rare- Identifiers
- MONDO:0060502 OMIM:617527Orphanet:521426
- Causal genes
- PLAA
- Part of
- Mendelian neurodevelopmental disorderCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- NDMSBA
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