OMOP Concept 44782850

Hereditary retinal dystrophy primarily involving retinal pigment epithelium

StandardConditionSNOMED698847000Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2014
Valid to
31 Dec 2099
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Source codes that map to this concept

1 source code normalizes to Hereditary retinal dystrophy primarily involving retinal pigment epithelium via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Hereditary retinal dystrophy primarily involving retinal pigment epithelium across source vocabularies.

  • distrofia hereditaria de la retina que afecta principalmente al epitelio pigmentario
  • distrofia hereditaria de la retina que afecta principalmente al epitelio pigmentario (trastorno)
  • Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder)
  • Inherited retinal dystrophy primarily involving retinal pigment epithelium

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Ordered by distance - 1 is a direct parent or child.

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