OBO ID: DOID:0110383
Term Name: retinitis pigmentosa 7 Search Ontology:
Synonyms:
  • RP7
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/1749427
References:
Ontology: Human Disease   (DOID:0110383)
OTHER retinitis pigmentosa 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PRPH2 Retinitis pigmentosa 7 and digenic form 608133
Leber congenital amaurosis 18 608133
ROM1 Retinitis pigmentosa 7, digenic form 608133
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None