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neurodevelopmental disorder with severe motor impairment and absent language

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Uniprot Description An autosomal dominant neurodevelopmental disorder characterized by global developmental delay, intellectual disability, severe speech impairment and gait abnormalities.
Mondo Term and Equivalent IDs
MONDO:0060622:  neurodevelopmental disorder with severe motor impairment and absent language
UMLS:C4540496: