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DO Term : cataract 33 [DOID:0110264] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in homozygous mutation in the beaded filament structural protein-1 gene (BFSP1) on chromosome 20p12.

synonyms:
CTRCT33,
OMIM:611391,
ICD10CM:Q12.0,
cortical cataract 33,
611391

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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