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DO Term : aniridia 1 [DOID:0070532] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An aniridia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13. Additional ocular anomalies are also common.

synonyms:
106210,
OMIM:106210

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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