OBO ID: DOID:0110377
Term Name: retinitis pigmentosa 49 Search Ontology:
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 retinitis pigmentosa 49 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CNGA1 Retinitis pigmentosa 49 613756
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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