Retinitis Pigmentosa [retinopathia pigmentosa]

topical
56
Terms

primární pigmentová degenerace
retinitis pigmentosa
tapetoretinální degenerace
typická retinopathia pigmentosa

 

Pigmentary Retinopathy
Tapetoretinal Degeneration

Persistent link   https://www.medvik.cz/link/D012174
Definition

Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.

Annotation
note entry term ROD CONE DYSTROPHIES: CONE-ROD DYSTROPHIES is also available
DUI
D012174 MeSH Browser
CUI
M0018960

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 5
CN
congenital 2
DI
diagnosis 12
DG
diagnostic imaging 1
DH
diet therapy
DT
drug therapy 1
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology
EH
ethnology
ET
etiology 3
GE
genetics 26
HI
history
IM
immunology
ME
metabolism 7
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 7
PP
physiopathology 3
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 3
TH
therapy 11
UR
urine
VE
veterinary 1
VI
virology

C Diseases
C11 Eye Diseases 1 491
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 58
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 56
C11.270.684.249 Alstrom Syndrome 1
C11.270.684.624 Bardet-Biedl Syndrome 19
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 404
C11.768.585 Retinal Degeneration 75
C11.768.585.658 Retinal Dystrophies 6
C11.768.585.658.250 Cone-Rod Dystrophies
C11.768.585.658.500 Retinitis Pigmentosa 56
C11.768.585.658.500.627 Kearns-Sayre Syndrome 11
C11.768.585.658.500.813 Usher Syndromes 8
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 214
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 58
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 56
C16.320.290.684.249 Alstrom Syndrome 1
C16.320.290.684.500 Usher Syndromes 8
C16.320.290.724 Stargardt Disease 6
C16.320.290.763 Vitelliform Macular Dystrophy 5
C16.320.290.842 Weill-Marchesani Syndrome 1

Aldred syndrome Disease MeSH Browser

Amaurosis hypertrichosis Disease MeSH Browser

Bork Stender Schmidt syndrome Disease MeSH Browser

Chang Davidson Carlson syndrome Disease MeSH Browser

Chromosome Xp11.3 Deletion Syndrome Disease MeSH Browser

Cone Dystrophy 3 Disease MeSH Browser

Cone Dystrophy 4 Disease MeSH Browser

Cone Dystrophy, X-Linked, 1 Disease MeSH Browser

Cone dystrophy, x-linked, with tapetal-like sheen Disease MeSH Browser

Cone rod dystrophy amelogenesis imperfecta Disease MeSH Browser

Cone-Rod Dystrophy 1 Disease MeSH Browser

Cone-Rod Dystrophy 10 Disease MeSH Browser

Cone-Rod Dystrophy 11 Disease MeSH Browser

Cone-Rod Dystrophy 12 Disease MeSH Browser

Cone-Rod Dystrophy 13 Disease MeSH Browser

Cone-Rod Dystrophy 3 Disease MeSH Browser

Cone-Rod Dystrophy 5 Disease MeSH Browser

Cone-Rod Dystrophy 7 Disease MeSH Browser

Cone-Rod Dystrophy 8 Disease MeSH Browser

Cone-Rod Dystrophy, X-Linked, 2 Disease MeSH Browser

Cone-Rod Dystrophy, X-Linked, 3 Disease MeSH Browser

Cone-Rod Dystrophy, X-Linked, Type 1 Disease MeSH Browser

Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness Disease MeSH Browser

Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Disease MeSH Browser

Flynn Aird syndrome Disease MeSH Browser

Furukawa Takagi Nakao syndrome Disease MeSH Browser

Hardikar syndrome Disease MeSH Browser

Leber Congenital Amaurosis 14 Disease MeSH Browser

Leber Congenital Amaurosis 3 Disease MeSH Browser

Light Fixation Seizure Syndrome Disease MeSH Browser

Mainzer-Saldino Disease Disease MeSH Browser

Meckel syndrome type 1 Disease MeSH Browser

Metaphyseal Chondrodysplasia with Retinitis Pigmentosa Disease MeSH Browser

Microcephaly, Retinitis Pigmentosa, and Sutural Cataract Disease MeSH Browser

Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen Disease MeSH Browser

Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus Disease MeSH Browser

Neuropathy ataxia and retinitis pigmentosa Disease MeSH Browser

Newfoundland Rod-Cone Dystrophy Disease MeSH Browser

Oculotrichodysplasia Disease MeSH Browser

Oliver-McFarlane syndrome Disease MeSH Browser

Pallidal Degeneration, Progressive, with Retinitis Pigmentosa Disease MeSH Browser

Peripheral Cone Dystrophy Disease MeSH Browser

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Disease MeSH Browser

Posterior column ataxia with retinitis pigmentosa Disease MeSH Browser

RHYNS syndrome Disease MeSH Browser

Radioulnar synostosis retinal pigment abnormalities Disease MeSH Browser

Retinal Cone Dystrophy 3A Disease MeSH Browser

Retinal Cone Dystrophy 3B Disease MeSH Browser

Retinal Cone Dystrophy 4 Disease MeSH Browser

Retinal cone dystrophy 2 Disease MeSH Browser

Retinitis Pigmentosa 10 Disease MeSH Browser

Retinitis Pigmentosa 11 Disease MeSH Browser

Retinitis Pigmentosa 12 Disease MeSH Browser

Retinitis Pigmentosa 13 Disease MeSH Browser

Retinitis Pigmentosa 14 Disease MeSH Browser

Retinitis Pigmentosa 17 Disease MeSH Browser

Retinitis Pigmentosa 18 Disease MeSH Browser

Retinitis Pigmentosa 19 Disease MeSH Browser

Retinitis Pigmentosa 2 Disease MeSH Browser

Retinitis Pigmentosa 20 Disease MeSH Browser

Retinitis Pigmentosa 25 Disease MeSH Browser

Retinitis Pigmentosa 26 Disease MeSH Browser

Retinitis Pigmentosa 27 Disease MeSH Browser

Retinitis Pigmentosa 29 Disease MeSH Browser

Retinitis Pigmentosa 3 Disease MeSH Browser

Retinitis Pigmentosa 30 Disease MeSH Browser

Retinitis Pigmentosa 31 Disease MeSH Browser

Retinitis Pigmentosa 32 Disease MeSH Browser

Retinitis Pigmentosa 33 Disease MeSH Browser

Retinitis Pigmentosa 34 Disease MeSH Browser

Retinitis Pigmentosa 35 Disease MeSH Browser

Retinitis Pigmentosa 36 Disease MeSH Browser

Retinitis Pigmentosa 37 Disease MeSH Browser

Retinitis Pigmentosa 4 Disease MeSH Browser

Retinitis Pigmentosa 41 Disease MeSH Browser

Retinitis Pigmentosa 42 Disease MeSH Browser

Retinitis Pigmentosa 46 Disease MeSH Browser

Retinitis Pigmentosa 6 Disease MeSH Browser

Retinitis Pigmentosa 7 Disease MeSH Browser

Retinitis Pigmentosa 7 With Bull'S-Eye Maculopathy Disease MeSH Browser

Retinitis Pigmentosa 7, Digenic Disease MeSH Browser

Retinitis Pigmentosa 9 Disease MeSH Browser

Retinitis Pigmentosa Inversa with Deafness Disease MeSH Browser

Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium Disease MeSH Browser

Retinitis Pigmentosa, Concentric Disease MeSH Browser

Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism Disease MeSH Browser

Retinitis Pigmentosa, Late-Adult Onset Disease MeSH Browser

Retinitis Pigmentosa, Late-Onset Dominant Disease MeSH Browser

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Disease MeSH Browser

Retinitis Pigmentosa, Y-Linked Disease MeSH Browser

Retinitis pigmentosa 1 Disease MeSH Browser

Retinopathy, Pericentral Pigmentary, Autosomal Recessive Disease MeSH Browser

Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa Disease MeSH Browser

Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction Disease MeSH Browser

Senior-Loken syndrome 4 Disease MeSH Browser

Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa Disease MeSH Browser

Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation Disease MeSH Browser

Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy Disease MeSH Browser

Tapetoretinal Degeneration with Ataxia Disease MeSH Browser

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