Search Ontology:
Human Disease

retinitis pigmentosa 49

Term ID
DOID:0110377
Synonyms
  • RP49
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12. https://www.ncbi.nlm.nih.gov/pubmed/7479749
References
Ontology
Human Disease   ( DOID:0110377 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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