Gyrate Atrophy [gyrátová atrofie]

topical
1
Terms

deficit ornitinaminotransferázy
deficit ornitinketoacidtransaminázy
hyperornitinemie s gyrátovou atrofií
ornitinemie s gyrátovou atrofií

 

Gyrate Atrophy of Choroid and Retina
Gyrate Atrophy of the Choroid and Retina
Hyperornithinemia with Gyrate Atrophy of Choroid and Retina
OAT Deficiency
OKT Deficiency
Ornithine Aminotransferase Deficiency
Ornithine Keto Acid Aminotransferase Deficiency
Ornithine Ketoacid Aminotransferase Deficiency
Ornithine-Delta-Aminotransferase Deficiency
Ornithinemia with Gyrate Atrophy

Persistent link   https://www.medvik.cz/link/D015799
Definition

Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.

Annotation
a hered eye dis; /congen permitted: read MeSH definition
DUI
D015799 MeSH Browser
CUI
M0024200
Previous indexing
Retinal Degeneration (1970-1989); Atrophy (1970-1989); Choroid (1970-1989)
History note
90
Public note
90

Allowable subheadings

BL
blood 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 0
CN
congenital 0
DI
diagnosis 0
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 1
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 0
EH
ethnology 0
ET
etiology 1
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 1
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
C11.270 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
C11.941 Uveal Diseases 47
C11.941.160 Choroid Diseases 16
C11.941.160.177 Choroid Hemorrhage 4
C11.941.160.238 Choroid Neoplasms 45
C11.941.160.241 Choroidal Effusions
C11.941.160.244 Choroidal Neovascularization 66
C11.941.160.300 Choroideremia 3
C11.941.160.478 Choroiditis 9
C11.941.160.578 Gyrate Atrophy 1
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
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

Add