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neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal recessive neurodevelopmental disorder characterized by severe developmental delay, intellectual disability, severe microcephaly, and cortical atrophy.
Mondo Term and Equivalent IDs
MONDO:0060621:  neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy
UMLS:C4540493: