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DO Term : cataract 13 with adult i phenotype [DOID:0110242] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.

synonyms:
116700,
ICD10CM:Q12.0,
CTRCT13,
OMIM:116700

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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