stargardt's disease

Preferred Label : stargardt's disease;

Details

Origin ID

DA-71908;

UMLS CUI

C0271093;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily A member 4 [ORDO Gene]
- ATP binding cassette subfamily A member 4 [HGNC gene]
- Hereditary retinal dystrophy [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Fundus flavimaculatus [PASCAL descriptor]
- Fundus flavimaculatus (disorder) [SNOMED CT concept]
- Stargardt Disease [MeSH concept]
- Stargardt Disease [MeSH Descriptor]
- Stargardt Disease [NCIt concept]
- Stargardt chorioretinal degeneration [PASCAL descriptor]
- Stargardt disease [DO Concept]
- Stargardt disease [Disease (Nov.)]
- Stargardt disease [ICD-11 More detail]
- Stargardt disease [ORDO Disease]
- Stargardt's disease [MedDRA Preferred Term]
- Stargardt's disease (disorder) [Inactive SNOMED CT concept]
- Stargardt's disease (disorder) [Inactive SNOMED CT concept]
- Stargardt's disease (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Hereditary retinal dystrophy [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic macular dystrophy [ORDO Disease]
Metaterm(s)
- ophthalmology [CISMeF Metaterm]
SNOMED CT concept
- Stargardt's disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Fundus flavimaculatus (disorder) [SNOMED CT concept]
- Stargardt Disease [MeSH Descriptor]
- Stargardt Disease [NCIt concept]
- Stargardt disease [Disease (Nov.)]
- Stargardt's disease [MedDRA Preferred Term]
- Stargardt's disease (disorder) [SNOMED CT concept]
- flavimacular retinopathy [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

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