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retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes

AttributesValues
rdf:type
description
  • Krankheit (de)
  • хвороба (uk)
  • retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes (en)
  • difficultés d'adaptation aux changements de luminosité (fr)
exact match
exact match
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
Mondo ID
  • MONDO_0012033
Disease Ontology ID
  • DOID:0050335
rdfs:label
  • bradyopsia (en)
  • bradyopsia (sv)
  • bradyopsie (fr)
skos:prefLabel
  • bradyopsia (en)
  • bradyopsia (sv)
  • bradyopsie (fr)
name
  • bradyopsia (en)
  • bradyopsia (sv)
  • bradyopsie (fr)
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H00973
UniProt disease ID
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
GARD rare disease ID
OMIM ID
UniProt disease ID
  • DI-02219
Orphanet ID
  • 75374
ICD-9-CM
  • 368.8
genetic association
ICD-10-CM
  • H53.8
GARD rare disease ID
  • 12299
OMIM ID
  • 608415
Human Phenotype Ontology ID
Human Phenotype Ontology ID
  • HP:0030511
skos:altLabel
  • PERRS (en)
  • Bradyopsia (en)
  • PROLONGED ELECTRORETINAL RESPONSE SUPPRESSION (en)
  • PROLONGED ELECTRORETINAL RESPONSE SUPPRESSION; PERRS (en)
UMLS CUI
MeSH descriptor ID
on focus list of Wikimedia project
MeSH descriptor ID
UMLS CUI
  • C1842073
MeSH descriptor ID
  • C564243
on focus list of Wikimedia project
is owl:sameAs of
is about of
is genetic association of
is genetic association of
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