Search Ontology:
Human Disease

retinitis pigmentosa 26

Term ID
DOID:0110368
Synonyms
  • RP26
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the CERKL gene on chromosome 2q31. https://www.ncbi.nlm.nih.gov/pubmed/14681825
References
Ontology
Human Disease   ( DOID:0110368 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models