Search Ontology:
Human Disease

retinitis pigmentosa 33

Term ID
DOID:0110366
Synonyms
  • RP33
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11. https://www.ncbi.nlm.nih.gov/pubmed/19878916
References
Ontology
Human Disease   ( DOID:0110366 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models