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DO Term : cone-rod dystrophy 10 [DOID:0111017] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22.

synonyms:
610283,
MESH:C564597,
OMIM:610283,
CORD10

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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