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DO Term : cataract 19 multiple types [DOID:0110263] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in homozygous mutation in the LIM2 gene on chromosome 19q13.

synonyms:
615277,
CTRCT19,
ICD10CM:Q12.0,
OMIM:615277

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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