OBO ID: DOID:0110406
Term Name: retinitis pigmentosa 30 Search Ontology:
Synonyms:
  • RP30
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25.https://www.ncbi.nlm.nih.gov/pubmed/14609921
References:
Ontology: Human Disease   (DOID:0110406)
Relationships
is a type of:
OTHER retinitis pigmentosa 30 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FSCN2 Retinitis pigmentosa 30 607921
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None