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DO Term : cataract 10 multiple types [DOID:0110258] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in heterozygous mutation in the CRYBA1 gene on chromosome 17q11.

synonyms:
OMIM:600881,
600881,
ICD10CM:Q12.0,
congenital zonular cataract with sutural opacities,
CCZS,
CTRCT10

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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