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DO Term : cataract 43 [DOID:0110259] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in heterozygous mutation in the UNC45B gene on chromosome 17q12.

synonyms:
CTRCT43,
616279,
ICD10CM:Q12.0,
OMIM:616279

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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