Telangiectasia, Hereditary Hemorrhagic [hereditární hemoragická teleangiektazie]

topical
34
Terms

dědičná hemoragická teleangiektazie
hemoragická hereditární teleangiektázie
hereditární hemoragická teleangiektazie Rendu-Osler
morbus Osler-Weber-Rendu
morbus Rendu-Osler
morbus Rendu-Osler-Weber
Oslerova-Renduova-Weberova nemoc
Rendu-Osler-Weberova choroba
Renduova-Oslerova nemoc
Renduova-Oslerova-Weberova choroba
Renduova-Oslerova-Weberova nemoc
teleangiectasia hereditaria haemorrhagica
teleangiektazie dědičná hemoragická

 

Hereditary Hemorrhagic Telangiectasia
Osler-Rendu Disease
Osler-Rendu-Weber Disease
Osler-Weber-Rendu Syndrome
Osler's Disease
Rendu-Osler-Weber Disease
Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber
Telangiectasia, Hereditary Hemorrhagic, Type 1
Weber-Osler Disease
Weber-Osler Syndrome

Persistent link   https://www.medvik.cz/link/D013683
Definition

An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA.

DUI
D013683 MeSH Browser
CUI
M0021123
History note
1968(1966); for OSLER-RENDU DISEASE use ANGIOMATOSIS 1963-1967
Public note
1968; for OSLER-RENDU DISEASE see ANGIOMATOSIS 1963-1967

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 1
CO
complications 9
DI
diagnosis 19
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 2
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology 4
EH
ethnology
ET
etiology 5
GE
genetics 5
HI
history
IM
immunology
ME
metabolism
MI
microbiology 1
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 4
PP
physiopathology 3
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 1
TH
therapy 10
UR
urine
VE
veterinary
VI
virology

C Diseases
C14 Cardiovascular Diseases 10 507
C14.907 Vascular Diseases 1 790
C14.907.454 Hemostatic Disorders 49
C14.907.454.140 Cryoglobulinemia 72
C14.907.454.240 Ehlers-Danlos Syndrome 51
C14.907.454.385 Hemangioma, Cavernous 53
C14.907.454.460 Multiple Myeloma 1 782
C14.907.454.530 Pseudoxanthoma Elasticum 13
C14.907.454.550 Purpura, Hyperglobulinemic 4
C14.907.454.800 Scurvy 28
C14.907.454.810 Shwartzman Phenomenon 10
C14.907.454.900 Telangiectasia, Hereditary Hemorrhagic 34
C14.907.454.960 Waldenstrom Macroglobulinemia 112
C14.907.823 Telangiectasis 57
C14.907.823.213 Ataxia Telangiectasia 47
C14.907.823.225 CREST Syndrome 6
C14.907.823.502 Retinal Telangiectasis 3
C14.907.823.780 Telangiectasia, Hereditary Hemorrhagic 34
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 975
C15.378.463 Hemorrhagic Disorders 95
C15.378.463.515 Hemostatic Disorders 49
C15.378.463.515.140 Cryoglobulinemia 72
C15.378.463.515.240 Ehlers-Danlos Syndrome 51
C15.378.463.515.385 Hemangioma, Cavernous 53
C15.378.463.515.460 Multiple Myeloma 1 782
C15.378.463.515.530 Pseudoxanthoma Elasticum 13
C15.378.463.515.550 Purpura, Hyperglobulinemic 4
C15.378.463.515.580 IgA Vasculitis 76
C15.378.463.515.800 Scurvy 28
C15.378.463.515.810 Shwartzman Phenomenon 10
C15.378.463.515.900 Telangiectasia, Hereditary Hemorrhagic 34
C15.378.463.515.960 Waldenstrom Macroglobulinemia 112
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
C16.131.240 Cardiovascular Abnormalities 91
C16.131.240.850 Vascular Malformations 56
C16.131.240.850.250 Congenital Portosystemic Shunt
C16.131.240.850.500 Arterio-Arterial Fistula 5
C16.131.240.850.750 Arteriovenous Malformations 149
C16.131.240.850.875 Central Nervous System Vascular Malformations 20
C16.131.240.850.890 May-Thurner Syndrome 5
C16.131.240.850.898 Median Arcuate Ligament Syndrome 6
C16.131.240.850.902 Persistent Left Superior Vena Cava 3
C16.131.240.850.906 Pulmonary Atresia 15
C16.131.240.850.937 Scimitar Syndrome 3
C16.131.240.850.952 Single Umbilical Artery
C16.131.240.850.968 Telangiectasia, Hereditary Hemorrhagic 34
C16.131.240.850.984 Vascular Ring

Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Disease MeSH Browser

Osler-rendu-weber syndrome 2 Disease MeSH Browser

Osler-rendu-weber syndrome 3 Disease MeSH Browser

Telangiectasia, Hereditary Hemorrhagic, Type 4 Disease MeSH Browser

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