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DO Term : cone-rod dystrophy 11 [DOID:0111018] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the RAX2 gene on chromosome 19p13.

synonyms:
OMIM:610381,
610381,
MESH:C563671,
CORD11

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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