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DO Term : cataract 22 multiple types [DOID:0110268] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B3 crystallin gene (CRYBB3) on chromosome 22q11.

synonyms:
autosomal recessive congenital nuclear cataract 2,
ICD10CM:Q12.0,
CATCN2,
CTRCT22,
OMIM:609741,
609741

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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