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DOID:0060572 - Ritscher-Schinzel syndrome 2
Disease Ontology Definition:A Ritscher-Schinzel syndrome that has_material_basis_in mutation in the CCDC22 gene on chromosome Xp11.
Synonyms:
Xenbase Genes : ccdc22
MONDO:0010499 - Ritscher-Schinzel syndrome 2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Ritscher-Schinzel syndrome (is_a)