Search Ontology:
Human Disease

retinitis pigmentosa 13

Term ID
DOID:0110403
Synonyms
  • RP13
Definition
A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3. https://www.ncbi.nlm.nih.gov/pubmed/11468273
References
Ontology
Human Disease   ( DOID:0110403 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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