Descriptors Found: 1
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 1 / 1 DeCS     
Descriptor English:   Hypoadrenocorticism, Familial 
Descriptor Spanish:   Insuficiencia Corticosuprarrenal Familiar 
Descriptor Portuguese:   Hipoadrenocorticismo Familiar 
Synonyms English:   AHC with Isolated Gonadotropin Deficiency
Addison Disease, X Linked
Addison Disease, X-Linked
Adrenal Hypoplasia, Congenital
Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
Adrenal Hypoplasia, X-linked
Complex Glycerol Kinase Deficiency
Congenital Adrenal Hypoplasia
Congenital Adrenal Hypoplasias
Cytomegalic Adrenocortical Hypoplasia
Cytomegalic Adrenocortical Hypoplasias
Familial Hypoadrenocorticism
Familial Hypoadrenocorticisms
Familial X linked Addison Disease
Familial X-linked Addison Disease
Hypoadrenocorticisms, Familial
Hypoplasia, Congenital Adrenal
X linked Adrenal Hypoplasia
X linked Congenital Adrenal Hypoplasia
X-Linked Addison Disease
X-linked Adrenal Hypoplasia
X-linked Congenital Adrenal Hypoplasia
Xp21 Contiguous Gene Deletion Syndrome  
Tree Number:   C19.053.500.263.500
Definition English:   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 
History Note English:   2018(2010) 
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:   56957 
Unique Identifier:   D000075262 

Occurrence in VHL: