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DO Term : chromosome 18q deletion syndrome [DOID:0060407] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A chromosomal deletion syndrome that has_material_basis_in a terminal deficiency or macrodeletion that is characterized by mental retardation and congenital malformations.

synonyms:
ICD10CM:Q93.5,
monosomy 18q,
deletion 18q,
601808,
OMIM:601808,
ORDO:1600,
18q- syndrome,
MESH:C536580

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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