| Descriptor English: | Familial Exudative Vitreoretinopathies | ||||||
| Descriptor Spanish: |
Vitreorretinopatías Exudativas Familiares
| ||||||
| Descriptor Portuguese: | Vitreorretinopatias Exsudativas Familiares | ||||||
| Descriptor French: | Vitréorétinopathies exsudatives familiales | ||||||
| Entry term(s): |
Exudative Vitreoretinopathy, Familial Familial Exudative Vitreoretinopathy Vitreoretinopathy, Familial Exudative X Linked Familial Exudative Vitreoretinopathy X-Linked Familial Exudative Vitreoretinopathy XL-FEVR |
||||||
| Tree number(s): |
C11.250.345 C11.270.238 C11.768.337 C16.131.384.424 C16.320.290.352 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000080345 | ||||||
| Scope note: | A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by FLUORESCEIN ANGIOGRAPHY. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene. |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Public MeSH Note: | 2020; FAMILIAL EXUDATIVE VITREORETINOPATHY was indexed under RETINAL DISEASES 2014-2019, and under EYE DISEASES, HEREDITARY 2019 |
||||||
| History Note: | 2020(2014) |
||||||
| DeCS ID: | 59102 | ||||||
| Unique ID: | D000080345 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2020/01/01 | ||||||
| Date of Entry: | 2019/07/08 | ||||||
| Revision Date: | 2019/04/08 |
-
-
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
|
|
Familial Exudative Vitreoretinopathies
- Preferred
X-Linked Familial Exudative Vitreoretinopathy
- Narrower
| Concept UI |
M000647112 |
| Scope note | A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by FLUORESCEIN ANGIOGRAPHY. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene. |
| Preferred term | Familial Exudative Vitreoretinopathies |
| Entry term(s) |
Exudative Vitreoretinopathy, Familial Familial Exudative Vitreoretinopathy Vitreoretinopathy, Familial Exudative |
| Concept UI |
M000648458 |
| Preferred term | X-Linked Familial Exudative Vitreoretinopathy |
| Entry term(s) |
X Linked Familial Exudative Vitreoretinopathy XL-FEVR |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
