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Ritscher-Schinzel syndrome 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any Ritscher-Schinzel syndrome in which the cause of the disease is a mutation in the CCDC22 gene.
Uniprot Description A form of Ritscher-Schinzel syndrome, a developmental malformation syndrome characterized by intellectual disability, cerebellar brain malformations, congenital heart defects, and craniofacial abnormalities.
Mondo Term and Equivalent IDs
MONDO:0010499:  Ritscher-Schinzel syndrome 2
UMLS:C4225419: