Exudative vitreoretinopathy 3

Preferred Label : Exudative vitreoretinopathy 3;

Symbol : EVR3;

CISMeF acronym : EVR3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of familial exudative vitreoretinopathy (FEVR), see EVR1 (133780).;

Inheritance : Autosomal dominant;

Prefixed ID : %605750;

Details

Origin ID

605750;

UMLS CUI

C1854002;

Broader ORDO disease(s)
- Familial exudative vitreoretinopathy [ORDO Disease]
Currated CISMeF NLP mapping
- exudative vitreoretinopathy 3 [DO Concept]
- exudative vitreoretinopathy 3 [MeSH concept]
- exudative vitreoretinopathy 3 [MeSH Supplementary Concept]
DO Cross reference
- exudative vitreoretinopathy 3 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Exudative vitreoretinopathy [HPO term]
- Reduced visual acuity [HPO term]
- Retinal detachment [HPO term]
- Retinal exudate [HPO term]
- Retinal fold [HPO term]
- Retinal hole [HPO term]
ORDO concept(s)
- Familial exudative vitreoretinopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- exudative vitreoretinopathy 3 [MeSH Supplementary Concept]
- exudative vitreoretinopathy 3 [MeSH concept]
Validated automatic mappings to NTBT
- Familial exudative vitreoretinopathy [ORDO Disease]

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