OBO ID: DOID:0080292
Term Name: retinitis pigmentosa 81 Search Ontology:
Synonyms:
Definition: A retinitis pigmentosa that has_material_basis_in homozygous mutation in the IFT43 gene on chromosome 14q24. https://pubmed.ncbi.nlm.nih.gov/28973684/
References:
Ontology: Human Disease   ( DOID:0080292 )
Relationships
is a type of:
OTHER retinitis pigmentosa 81 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
IFT43 ?Retinitis pigmentosa 81 617871
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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