KEGG   DISEASE: Adrenal insufficiency, NR5A1 related
Entry
H02316                      Disease                                
Name
Adrenal insufficiency, NR5A1 related
Description
NR5A1, also termed steroidogenic factor 1 (SF-1), is a nuclear receptor and a key transcriptional regulator of genes involved in the hypothalamic-pituitary-steroidogenic axis. There are some known mutations of the NR5A1 gene in humans. A few of them were originally identified in patients with adrenal insufficiency. In 46,XY individuals, NR5A1-related phenotypes may range from disorders of sex development (DSD) to oligo/azoospermia, and in 46,XX individuals, from 46,XX ovotesticular and testicular DSD to primary ovarian insufficiency.
Category
Endocrine and metabolic disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 05 Endocrine, nutritional or metabolic diseases
  Endocrine diseases
   Disorders of the adrenal glands or adrenal hormone system
    5A74  Adrenocortical insufficiency
     H02316  Adrenal insufficiency, NR5A1 related
Pathway-based classification of diseases [BR:br08402]
 Endocrine system
  nt06310  CRH-ACTH-cortisol signaling
   H02316  Adrenal insufficiency, NR5A1 related
Pathway
hsa04927  Cortisol synthesis and secretion
Network
nt06310 CRH-ACTH-cortisol signaling
Gene
NR5A1 [HSA:2516] [KO:K08560]
Other DBs
ICD-11: 5A74.Y
ICD-10: E27.8
MeSH: C566130
OMIM: 612964
Reference
  Authors
Achermann JC, Ozisik G, Ito M, Orun UA, Harmanci K, Gurakan B, Jameson JL
  Title
Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner.
  Journal
J Clin Endocrinol Metab 87:1829-33 (2002)
DOI:10.1210/jcem.87.4.8376
Reference
  Authors
Lourenco D, Brauner R, Lin L, De Perdigo A, Weryha G, Muresan M, Boudjenah R, Guerra-Junior G, Maciel-Guerra AT, Achermann JC, McElreavey K, Bashamboo A
  Title
Mutations in NR5A1 associated with ovarian insufficiency.
  Journal
N Engl J Med 360:1200-10 (2009)
DOI:10.1056/NEJMoa0806228
Reference
  Authors
Domenice S, Machado AZ, Ferreira FM, Ferraz-de-Souza B, Lerario AM, Lin L, Nishi MY, Gomes NL, da Silva TE, Silva RB, Correa RV, Montenegro LR, Narciso A, Costa EM, Achermann JC, Mendonca BB
  Title
Wide spectrum of NR5A1-related phenotypes in 46,XY and 46,XX individuals.
  Journal
Birth Defects Res C Embryo Today 108:309-320 (2016)
DOI:10.1002/bdrc.21145
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