OBO ID: DOID:0112146
Term Name: retinitis pigmentosa 89 Search Ontology:
Synonyms:
  • RP89
Definition: A retinitis pigmentosa characterized by onset of retinitis pigmentosa in the first decade of life and additional features of ciliopathy that has_material_basis_in heterozygous mutation in the KIF3B gene on chromosome 20q11.21. https://pubmed.ncbi.nlm.nih.gov/32386558/
References:
Ontology: Human Disease   ( DOID:0112146 )
Relationships
is a type of:
OTHER retinitis pigmentosa 89 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KIF3B Retinitis pigmentosa 89 618955
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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