Ritscher-Schinzel syndrome 2 Disease Ontology Browser

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Disease Ontology Browser

Ritscher-Schinzel syndrome 2 (DOID:0060572)
Alliance: disease page
Alt IDs: OMIM:300963, ORDO:7
Definition: A Ritscher-Schinzel syndrome that has_material_basis_in mutation in the CCDC22 gene on chromosome Xp11.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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