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DO Term : cataract 40 [DOID:0110272] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cataract that has_material_basis_in mutation in the NHS gene on chromosome Xp22.

synonyms:
OMIM:302200,
cataract 40 X-linked,
302200,
ICD10CM:Q12.0,
CTRCT40,
cataract 40 with or without microcornea

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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