OBO ID: DOID:0110352
Term Name: retinitis pigmentosa 59 Search Ontology:
Synonyms:
  • RP59
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11. https://www.ncbi.nlm.nih.gov/pubmed/21295283
References:
Ontology: Human Disease   ( DOID:0110352 )
Relationships
is a type of:
OTHER retinitis pigmentosa 59 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DHDDS ?Congenital disorder of glycosylation, type 1bb 613861
Retinitis pigmentosa 59 613861
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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