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Inherited ocular disorder characterized by the loss of cone cells

Property Value
dbo:description
  • Krankheit (de)
  • хвороба (uk)
  • maladie de l'oeuil (fr)
  • Глазное расстройство по причине наследственности (ru)
  • malaltia hereditària que afecta a l'ull i provoca pèrdua de visió (ca)
  • inherited ocular disorder characterized by the loss of cone cells (en)
dbo:icd10
  • H35.5
dbo:omim
  • 300085 (xsd:integer)
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dbp:caption
  • Fundus of a 45 year-old patient with cone rod dystrophy segregating with a loss-of-function mutation in ABCA4. Note the presence of various-shaped pigment deposits in the posterior pole with atrophy of the retina, while the retina appears less damaged in periphery . (en)
dbp:icd
  • (en)
  • H35.5 (en)
dbp:name
  • Cone dystrophy (en)
dbp:omim
  • 300085 (xsd:integer)
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dct:subject
gold:hypernym
rdf:type
rdfs:label
  • Cone dystrophy (en)
  • Distròfia de cons i bastons (ca)
  • حثل المخروطية (ar)
  • Distrofia de conos y bastones (es)
  • Zapfen-Stäbchen-Dystrophie (de)
  • Distrofia di coni e bastoncelli (it)
  • Дистрофия колбочек (ru)
  • Tappdystrofi (sv)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Cone dystrophy (en)
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