Search on: GENETIC DISEASES, INBORN 
Descriptors Found: 1
Displaying: 1 .. 1  

 1 / 1 DeCS     
Descriptor English:   Genetic Diseases, Inborn 
Descriptor Spanish:   Enfermedades Genéticas Congénitas 
Descriptor Portuguese:   Doenças Genéticas Inatas 
Synonyms English:   Hereditary Diseases  
Tree Number:   C16.320
Definition English:   Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. 
Indexing Annotation English:   GEN only: prefer /genet with specific diseases; Manual 23.22+; Manual 19.8.34
See Related English:   Genetics, Medical
 
History Note English:   2002 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
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
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   6702 
Unique Identifier:   D030342 

Occurrence in VHL:
 

Similar:

 
DeCS CID-10 SciELO LILACS LIS