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DO Term : Newfoundland cone-rod dystrophy [DOID:0111015] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26.

synonyms:
607476,
NFRCD,
OMIM:607476

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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