OBO ID: DOID:0111015
Term Name: Newfoundland cone-rod dystrophy Search Ontology:
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 Newfoundland cone-rod dystrophy PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RLBP1 Newfoundland rod-cone dystrophy 607476
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None