Familial Exudative Vitreoretinopathies [familiární exsudativní vitreoretinopatie]

topical
Terms

familiární exsudativní vitreoretinopatie vázaná na chromozom X
XL-FEVR

 

Familial Exudative Vitreoretinopathy
X-Linked Familial Exudative Vitreoretinopathy
XL-FEVR

Persistent link   https://www.medvik.cz/link/D000080345
Definition

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.

DUI
D000080345 MeSH Browser
CUI
M000647112
History note
2020(2014)
Public note
2020; FAMILIAL EXUDATIVE VITREORETINOPATHY was indexed under RETINAL DISEASES 2014-2019, and under EYE DISEASES, HEREDITARY 2019

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BL
blood 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 0
DI
diagnosis 0
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 0
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 0
EH
ethnology 0
ET
etiology 0
GE
genetics 0
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 0
PP
physiopathology 0
PC
prevention & control 0
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 0
TH
therapy 0
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C11 Eye Diseases 1 485
C11.250 Eye Abnormalities 107
C11.250.060 Aniridia 18
C11.250.080 Anophthalmos 16
C11.250.090 Blepharophimosis 5
C11.250.105 Choroidal Effusions
C11.250.110 Coloboma 14
C11.250.300 Ectopia Lentis 3
C11.250.345 Familial Exudative Vitreoretinopathies
C11.250.390 Fraser Syndrome 2
C11.250.480 Hydrophthalmos 9
C11.250.566 Microphthalmos 17
C11.250.616 Persistent Hyperplastic Primary Vitreous 7
C11.250.666 Retinal Dysplasia 4
C11.270 Eye Diseases, Hereditary 57
C11.270.019 Aicardi Syndrome
C11.270.040 Albinism 17
C11.270.060 Aniridia 18
C11.270.142 Choroideremia 3
C11.270.147 Coloboma 14
C11.270.151 Cone Dystrophy
C11.270.152 Cone-Rod Dystrophies
C11.270.162 Corneal Dystrophies, Hereditary 63
C11.270.235 Duane Retraction Syndrome 9
C11.270.238 Familial Exudative Vitreoretinopathies
C11.270.240 Graves Ophthalmopathy 57
C11.270.468 Gyrate Atrophy 1
C11.270.516 Leber Congenital Amaurosis 6
C11.270.564 Optic Atrophies, Hereditary 5
C11.270.588 Optic Nerve Hypoplasia 1
C11.270.612 Retinal Degeneration 75
C11.270.660 Retinal Dysplasia 4
C11.270.684 Retinitis Pigmentosa 55
C11.270.862 Retinoblastoma 159
C11.270.872 Stargardt Disease 6
C11.270.881 Walker-Warburg Syndrome 4
C11.270.921 Weill-Marchesani Syndrome 1
C11.768 Retinal Diseases 402
C11.768.094 Angioid Streaks 2
C11.768.175 Central Serous Chorioretinopathy 14
C11.768.216 Cone Dystrophy
C11.768.257 Diabetic Retinopathy 859
C11.768.328 Epiretinal Membrane 31
C11.768.337 Familial Exudative Vitreoretinopathies
C11.768.346 Hypertensive Retinopathy 13
C11.768.364 Leber Congenital Amaurosis 6
C11.768.400 Retinal Artery Occlusion 53
C11.768.585 Retinal Degeneration 75
C11.768.648 Retinal Detachment 275
C11.768.660 Retinal Dysplasia 4
C11.768.710 Retinal Hemorrhage 51
C11.768.717 Retinal Neoplasms 30
C11.768.725 Retinal Neovascularization 45
C11.768.740 Retinal Perforations 44
C11.768.748 Retinal Telangiectasis 3
C11.768.757 Retinal Vasculitis 19
C11.768.760 Retinal Vein Occlusion 77
C11.768.773 Retinitis 49
C11.768.836 Retinopathy of Prematurity 137
C11.768.863 Foveomacular Retinitis
C11.768.890 Vitreoretinopathy, Proliferative 22
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 740
C16.131.384 Eye Abnormalities 107
C16.131.384.079 Aniridia 18
C16.131.384.159 Anophthalmos 16
C16.131.384.190 Blepharophimosis 5
C16.131.384.282 Coloboma 14
C16.131.384.405 Ectopia Lentis 3
C16.131.384.424 Familial Exudative Vitreoretinopathies
C16.131.384.442 Fraser Syndrome 2
C16.131.384.480 Hydrophthalmos 9
C16.131.384.666 Microphthalmos 17
C16.131.384.725 Persistent Hyperplastic Primary Vitreous 7
C16.131.384.784 Retinal Dysplasia 4
C16.320 Genetic Diseases, Inborn 1 213
C16.320.290 Eye Diseases, Hereditary 57
C16.320.290.019 Aicardi Syndrome
C16.320.290.040 Albinism 17
C16.320.290.078 Aniridia 18
C16.320.290.142 Choroideremia 3
C16.320.290.152 Cone-Rod Dystrophies
C16.320.290.162 Corneal Dystrophies, Hereditary 63
C16.320.290.235 Duane Retraction Syndrome 9
C16.320.290.352 Familial Exudative Vitreoretinopathies
C16.320.290.410 Graves Ophthalmopathy 57
C16.320.290.468 Gyrate Atrophy 1
C16.320.290.564 Optic Atrophies, Hereditary 5
C16.320.290.612 Optic Nerve Hypoplasia 1
C16.320.290.660 Retinal Dysplasia 4
C16.320.290.684 Retinitis Pigmentosa 55
C16.320.290.724 Stargardt Disease 6
C16.320.290.763 Vitelliform Macular Dystrophy 5
C16.320.290.842 Weill-Marchesani Syndrome 1

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