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DO Term : cataract 48 [DOID:0070354] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment.

synonyms:
CTRCT48,
618415,
OMIM:618415

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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