Search on: TELANGIECTASIA, HEREDITARY HEMORRHAGIC 
Descriptors Found: 1
Displaying: 1 .. 1  

 1 / 1 DeCS     
Descriptor English:   Telangiectasia, Hereditary Hemorrhagic 
Descriptor Spanish:   Telangiectasia Hemorrágica Hereditaria 
Descriptor Portuguese:   Telangiectasia Hemorrágica Hereditária 
Synonyms English:   Hereditary Hemorrhagic Telangiectasia
Osler's Disease
Osler-Rendu-Weber Disease
Osler-Weber-Rendu Syndrome
Rendu-Osler-Weber
Telangiectasia, Hereditary Hemorrhagic, Type 1
Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber
Weber-Osler
Disease, Osler's
Hemorrhagic Telangiectasia, Hereditary
Osler Disease
Osler Rendu Disease
Osler Rendu Weber Disease
Osler Weber Rendu Syndrome
Rendu Osler Weber
Weber Osler
Osler-Rendu Disease  
Tree Number:   C14.907.454.900
C14.907.823.780
C15.378.463.515.900
C16.131.240.850.968
Definition English:   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. 
History Note English:   1968(1966); for OSLER-RENDU DISEASE use ANGIOMATOSIS 1963-1967 
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:   14061 
Unique Identifier:   D013683 

Occurrence in VHL:
 
LILACS    
MEDLINE    
BBO    
HomeoIndex    
MedCarib    
IBECS    

Similar:

 
DeCS CID-10 LILACS