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neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal recessive neurodevelopmental disorder characterized by progressive microcephaly, spastic quadriparesis, global developmental delay, profound mental retardation and severely impaired or absent motor function. More variable features include seizures and optic atrophy.
Mondo Term and Equivalent IDs
MONDO:0060502:  neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
Orphanet:521426: 
UMLS:C4479631: