A Ritscher-Schinzel syndrome that has_material_basis_in mutation in the CCDC22 gene on chromosome Xp11. [ url:https://www.ncbi.nlm.nih.gov/pubmed/24916641 http://purl.obolibrary.org/obo/ECO_0007645 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ORDO:7
  • MIM:300963
Subsets

DO_rare_slim

has obo namespace

disease_ontology

id

DOID:0060572