amaurosis congenita of leber, type 2

Preferred Label : amaurosis congenita of leber, type 2;

MeSH synonym : leber congenital amaurosis type 2; amaurosis congenita of leber ii; leber congenital amaurosis 2;

Details

Origin ID

C536601;

UMLS CUI

C1859844;

Automatic exact mappings (from CISMeF team)
- Leber congenital amaurosis [ORDO Disease]
- Leber congenital amaurosis 1 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Leber congenital amaurosis 2 [DO Concept]
- Leber congenital amaurosis 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- leber congenital amaurosis [MeSH Descriptor]
Record concept(s)
- Amaurosis congenita of Leber, type 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Leber congenital amaurosis 2 [OMIM Phenotype]
- Leber congenital amaurosis 2 [DO Concept]

Keyword's position in hierarchy(ies) :

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