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Descriptor English: Familial Exudative Vitreoretinopathies
Descriptor Spanish: Vitreorretinopatías Exudativas Familiares
Descriptor Portuguese: Vitreorretinopatias Exsudativas Familiares
Descriptor French: Without translation
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
Familial Exudative Vitreoretinopathies - Preferred
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
X-Linked Familial Exudative Vitreoretinopathy - Narrower
Concept UI M000648458
Preferred term X-Linked Familial Exudative Vitreoretinopathy
Entry term(s) X Linked Familial Exudative Vitreoretinopathy
XL-FEVR



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