OBO ID: DOID:0112145
Term Name: retinitis pigmentosa 88 Search Ontology:
Synonyms:
  • RP88
Definition: A retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that has_material_basis_in homozygous or compound heterozygous mutation in the RP1L1 gene on chromosome 8p23.1. (3)
References:
Ontology: Human Disease   ( DOID:0112145 )
Relationships
is a type of:
OTHER retinitis pigmentosa 88 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RP1L1 Retinitis pigmentosa 88 618826
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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