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- Glucocorticoid_deficiency_1 abstract "Familial glucocorticoid deficiency (FGD or GCCD) is an adrenocortical failure characterized by low levels of plasma cortisol produced by the adrenal gland despite high levels of plasma ACTH. This is an inherited disorder with several different causes which define the type.FGD type 1 (FGD1 or GCCD1) is caused by mutations in the ACTH receptor (melanocortin 2 receptor; MC2R). FGD type 2 is caused by mutations in the MC2R accessory protein (MRAP). These two types account for 45% of all cases of FGD.Some cases of FGD type 3 are caused by mutations in the steroidogenic acute regulatory protein (StAR), with similarity to the nonclassic form of lipoid congenital adrenal hyperplasia. In this case, a general impairment in not just adrenal steroid production, but gonadal steroid production can affect sexual development and fertility.The causes of other cases of FGD type 3 not due to StAR are currently unknown.".
- Glucocorticoid_deficiency_1 wikiPageID "3809232".
- Glucocorticoid_deficiency_1 wikiPageLength "2891".
- Glucocorticoid_deficiency_1 wikiPageOutDegree "9".
- Glucocorticoid_deficiency_1 wikiPageRevisionID "591476127".
- Glucocorticoid_deficiency_1 wikiPageWikiLink ACTH_receptor.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Adrenal_cortex.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Adrenal_gland.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Adrenocorticotropic_hormone.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Category:Adrenal_gland_disorders.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Cortisol.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Lipoid_congenital_adrenal_hyperplasia.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Melanocortin_2_receptor_accessory_protein.
- Glucocorticoid_deficiency_1 wikiPageWikiLink Steroidogenic_acute_regulatory_protein.
- Glucocorticoid_deficiency_1 wikiPageWikiLinkText "Familial glucocorticoid deficiency".
- Glucocorticoid_deficiency_1 wikiPageWikiLinkText "Glucocorticoid deficiency 1".
- Glucocorticoid_deficiency_1 wikiPageWikiLinkText "glucocorticoid deficiency 1".
- Glucocorticoid_deficiency_1 wikiPageUsesTemplate Template:Endocrine-disease-stub.
- Glucocorticoid_deficiency_1 wikiPageUsesTemplate Template:OMIM.
- Glucocorticoid_deficiency_1 wikiPageUsesTemplate Template:Reflist.
- Glucocorticoid_deficiency_1 subject Category:Adrenal_gland_disorders.
- Glucocorticoid_deficiency_1 hypernym Failure.
- Glucocorticoid_deficiency_1 type MilitaryConflict.
- Glucocorticoid_deficiency_1 type Disorder.
- Glucocorticoid_deficiency_1 comment "Familial glucocorticoid deficiency (FGD or GCCD) is an adrenocortical failure characterized by low levels of plasma cortisol produced by the adrenal gland despite high levels of plasma ACTH. This is an inherited disorder with several different causes which define the type.FGD type 1 (FGD1 or GCCD1) is caused by mutations in the ACTH receptor (melanocortin 2 receptor; MC2R). FGD type 2 is caused by mutations in the MC2R accessory protein (MRAP).".
- Glucocorticoid_deficiency_1 label "Glucocorticoid deficiency 1".
- Glucocorticoid_deficiency_1 sameAs Q5572316.
- Glucocorticoid_deficiency_1 sameAs m.0b12s9.
- Glucocorticoid_deficiency_1 sameAs Q5572316.
- Glucocorticoid_deficiency_1 wasDerivedFrom Glucocorticoid_deficiency_1?oldid=591476127.
- Glucocorticoid_deficiency_1 isPrimaryTopicOf Glucocorticoid_deficiency_1.