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Details on Person adrenal gland disease

Class:IdDisease:5600600
_displayNameadrenal gland disease
_timestamp2014-06-12 12:42:50
created[InstanceEdit:5600601] Jassal, Bijay, 2014-06-12
definitionAn endocrine system disease that is located_in the adrenal gland.
identifier9553
modified[InstanceEdit:5600612] Jassal, Bijay, 2014-06-12
nameadrenal gland disease
referenceDatabase[ReferenceDatabase:1247631] DOID
(disease)[Pathway:5579017] Defective CYP11B1 causes AH4 [Homo sapiens]
[Pathway:5579021] Defective CYP21A2 causes AH3 [Homo sapiens]
[Pathway:5579028] Defective CYP17A1 causes AH5 [Homo sapiens]
[Pathway:5579031] Defective ACTH causes obesity and POMCD [Homo sapiens]
[FailedReaction:5580292] Defective CYP11B1 does not oxidise 11DCORT [Homo sapiens]
[FailedReaction:5601843] Defective CYP17A1 does not 17-hydroxylate PREG [Homo sapiens]
[FailedReaction:5601976] Defective CYP21A2 does not 21-hydroxylate PROG [Homo sapiens]
[FailedReaction:5603251] Defective ACTH does not bind MCR2 [Homo sapiens]
[FailedReaction:9035954] Defective CYP17A1 does not 17-hydroxylate P4 [Homo sapiens]
[FailedReaction:9035956] Defective CYP17A1 does not cleave 17aHPROG [Homo sapiens]
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No pathways have been reviewed or authored by adrenal gland disease (5600600)