Hereditary choroidal dystrophy

Preferred Label : Hereditary choroidal dystrophy;

ICD-10 exclusion note : ornithinemia (E72.4); hyperornithinemia (E72.4);

Rare : true;

Diag associé à un acte (%) : 0.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

H312;

UMLS CUI

C0154893;

Automatic exact mappings (from CISMeF team)
- Choroideremia [NCIt concept]
- Hereditary choroidal dystrophy [MedDRA Preferred Term]
- choroideremia [MeSH concept]
DO Cross reference
- hereditary choroidal atrophy [DO Concept]
ICD-10 exclusion(s)
- Disorders of ornithine metabolism [ICD-10 Sub-category]
Orphanet concepts
- Central areolar choroidal dystrophy [ORDO Disease]
- Choroideremia [ORDO Disease]
- Helicoid peripapillary chorioretinal degeneration [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Choroidal dystrophy [ICD-11 Category]
- Hereditary choroidal dystrophies [ICD-9 code]
- Hereditary choroidal dystrophy [MedDRA Preferred Term]
- Hereditary choroidal dystrophy (disorder) [SNOMED CT concept]
- Hereditary choroidal dystrophy or atrophy, unspecified [ICD-9 code]
- hereditary choroidal atrophy [DO Concept]
- hereditary choroidal dystrophy, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- choroideremia [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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