Stargardt disease

Preferred Label : Stargardt disease;

ICD-11 definition : Stargardt's disease is a form of juvenile hereditary macular degeneration characterized by discrete yellowish round or pisciform flecks around the macula at the level of the retinal pigment epithelium (rpe). Stargardt's disease is the most common hereditary macular dystrophy.;

ICD-11 synonym : Fundus flavimaculatus;

Details

Origin ID

1690038580;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily A member 4 [ORDO Gene]
- ATP binding cassette subfamily A member 4 [HGNC gene]
Currated CISMeF NLP mapping
- Fundus flavimaculatus [PASCAL descriptor]
- Fundus flavimaculatus (disorder) [SNOMED CT concept]
- Stargardt Disease [NCIt concept]
- Stargardt Disease [MeSH concept]
- Stargardt Disease [MeSH Descriptor]
- Stargardt chorioretinal degeneration [PASCAL descriptor]
- Stargardt disease [ORDO Disease]
- Stargardt disease [DO Concept]
- Stargardt disease 1 [OMIM Phenotype]
- Stargardt's disease [MedDRA Preferred Term]
- Stargardt's disease (disorder) [SNOMED CT concept]
- fundus flavimaculatus [SNOMED Notion]
- stargardt's disease [SNOMED Notion]

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