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neurodevelopmental disorder with microcephaly, ataxia, and seizures

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive disorder characterized by delayed psychomotor development, intellectual disability, seizures apparent in infancy, impaired speech, and aggressive behavior. Additional features include microcephaly, ataxia, and muscle weakness.
Mondo Term and Equivalent IDs
MONDO:0060577:  neurodevelopmental disorder with microcephaly, ataxia, and seizures
UMLS:C4540188: