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DO Term : chromosome 22q11.2 deletion syndrome, distal [DOID:0060413] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 22q11.2 region, distinct from DiGeorge syndrome and velocardiofacial syndrome.

synonyms:
DiGeorge syndrome and Velocardiofacial syndrome,
distal 22q11.2 microdeletion syndrome,
MESH:C567511,
OMIM:611867,
ORDO:261330,
611867

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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