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 MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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