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Okur-Chung neurodevelopmental syndrome

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal dominant neurodevelopmental disorder characterized by developmental delay, intellectual disability, behavioral problems, hypotonia, speech problems, microcephaly, pachygyria and variable dysmorphic features.
Mondo Term and Equivalent IDs
MONDO:0014893:  Okur-Chung neurodevelopmental syndrome
UMLS:C4310739: