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DO Term : Ritscher-Schinzel syndrome 2 [DOID:0060572] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Ritscher-Schinzel syndrome that has_material_basis_in mutation in the CCDC22 gene on chromosome Xp11.

synonyms:
ORDO:7,
OMIM:300963,
300963

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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