Pesquisa sobre: MFN=56957 
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Descritor Inglês:   Hypoadrenocorticism, Familial 
Descritor Espanhol:   Insuficiencia Corticosuprarrenal Familiar 
Descritor Português:   Hipoadrenocorticismo Familiar 
Sinônimos Inglês:   AHC with Isolated Gonadotropin Deficiency
Addison Disease, X-Linked
Adrenal Hypoplasia, Congenital
Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
Complex Glycerol Kinase Deficiency
Cytomegalic Adrenocortical Hypoplasia
Familial X-linked Addison Disease
X-linked Adrenal Hypoplasia
X-linked Congenital Adrenal Hypoplasia
Xp21 Contiguous Gene Deletion Syndrome
Addison Disease, X Linked
Adrenal Hypoplasia, X-linked
Congenital Adrenal Hypoplasia
Congenital Adrenal Hypoplasias
Cytomegalic Adrenocortical Hypoplasias
Familial Hypoadrenocorticism
Familial Hypoadrenocorticisms
Familial X linked Addison Disease
Hypoadrenocorticisms, Familial
Hypoplasia, Congenital Adrenal
X linked Adrenal Hypoplasia
X linked Congenital Adrenal Hypoplasia
X-Linked Addison Disease  
Categoria:   C19.053.500.263.500
Definição Inglês:   Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200 
Nota Histórica Inglês:   2018(2010) 
Qualificadores Permitidos Inglês:  
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
Número do Registro:   56957 
Identificador Único:   D000075262 

Ocorrência na BVS:
 
MEDLINE    

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