OBO ID: DOID:0110360
Term Name: retinitis pigmentosa 39 Search Ontology:
Synonyms:
  • RP39
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the USH2A gene on chromosome 1q41. https://www.ncbi.nlm.nih.gov/pubmed/12427073
References:
Ontology: Human Disease   ( DOID:0110360 )
Relationships
is a type of:
OTHER retinitis pigmentosa 39 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
USH2A Retinitis pigmentosa 39 613809
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.