Search on: MFN=59102 
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Descriptor English:   Familial Exudative Vitreoretinopathies 
Descriptor Spanish:   Vitreorretinopatías Exudativas Familiares 
Descriptor Portuguese:   Vitreorretinopatias Exsudativas Familiares 
Synonyms English:   Exudative Vitreoretinopathy, Familial
Familial Exudative Vitreoretinopathy
Vitreoretinopathy, Familial Exudative
X Linked Familial Exudative Vitreoretinopathy
X-Linked Familial Exudative Vitreoretinopathy
XL-FEVR  
Tree Number:   C11.250.345
C11.270.238
C11.768.337
C16.131.384.424
C16.320.290.352
Definition English:   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. 
History Note English:   2020(2014) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   59102 
Unique Identifier:   D000080345 

Occurrence in VHL:
 

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