Leber congenital amaurosis

Preferred Label : Leber congenital amaurosis;

ICD-11 definition : Leber congenital amaurosis (LCA) is a genetic retinal dystrophy and/or dysplasia of prenatal onset and is one of the frequent causes of childhood blindness.;

ICD-11 inclusion : Leber amaurosis;

Détails

Origin ID

650490256;

Automatic exact mappings (from CISMeF team)
- Leber amaurosis [PASCAL descriptor]
Currated CISMeF NLP mapping
- Leber Congenital Amaurosis [NCIt concept]
- Leber congenital amaurosis [DO Concept]
- Leber congenital amaurosis [ORDO Disease]
- Leber congenital amaurosis [OMIM phenotypic series]
- Leber congenital amaurosis [Disease (Nov.)]
- Leber's amaurosis (disorder) [SNOMED CT concept]
- Leber's congenital amaurosis [MedDRA Preferred Term]
- leber congenital amaurosis [MeSH Descriptor]
- leber congenital amaurosis [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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