Search Ontology:
Human Disease

Newfoundland cone-rod dystrophy

Term ID
DOID:0111015
Synonyms
  • NFRCD
Definition
A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26. https://www.ncbi.nlm.nih.gov/pubmed/11868161
References
Ontology
Human Disease   ( DOID:0111015 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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