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DO Term : cone-rod dystrophy 21 [DOID:0081447] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DRAM2 gene on chromosome 1p13.

synonyms:
616502,
OMIM:616502

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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