exudative vitreoretinopathy 1

Preferred Label : exudative vitreoretinopathy 1;

MeSH synonym : Exudative vitreoretinopathy, familial, autosomal dominant; Fevr, Autosomal Dominant; Criswick-Schepens syndrome;

Details

Origin ID

C536382;

UMLS CUI

C1851402;

Currated CISMeF NLP mapping
- Exudative Vitreoretinopathy 1 [NCIt concept]
- Exudative vitreoretinopathy 1 [OMIM Phenotype]
- Familial exudative vitreoretinopathy [ORDO Disease]
- exudative vitreoretinopathy 1 [DO Concept]
MeSH term(s) associated for indexing
- Familial Exudative Vitreoretinopathies [MeSH Descriptor]
- osteoporosis [MeSH Descriptor]
- vitreoretinopathy, proliferative [MeSH Descriptor]
ORDO relation(s)
- Familial exudative vitreoretinopathy [ORDO Disease]
Record concept(s)
- Exudative vitreoretinopathy 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Exudative Vitreoretinopathy 1 [NCIt concept]
- Exudative vitreoretinopathy 1 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Familial exsudative vitreoretinopathy [PASCAL descriptor]
- Familial exudative vitreoretinopathy [ICD-11 More detail]
- Familial exudative vitreoretinopathy (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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