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DO Term : chromosome 1q41-q42 deletion syndrome [DOID:0060412] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 1q41-q42 region.

synonyms:
612530,
1q41q42 microdeletion syndrome,
GARD:3738,
ICD10CM:Q93.5,
ORDO:250999,
1q41-q42 microdeletion syndrome,
OMIM:612530

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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