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DO Term : chromosome 18p deletion syndrome [DOID:0060406] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A chromosomal deletion syndrome that has_material_basis_in partial or complete deletion of the short arm of chromosome 18.

synonyms:
ORDO:1598,
De Grouchy syndrome,
18p- syndrome,
SNOMEDCT_US_2023_03_01:205632001,
MESH:C538309,
146390,
OMIM:146390,
GARD:8631,
UMLS_CUI:C0432442,
NCI:C84521,
monosomy 18p

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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