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Pathway
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Entries
Defective CYP21A2 causes AH3
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authored
[InstanceEdit:5579003] Jassal, Bijay, 2014年06月06日
created
[InstanceEdit:5579003] Jassal, Bijay, 2014年06月06日
crossReference
[DatabaseIdentifier:11944997] Mondo:0005495
dbId
5579021
disease
[Disease:5600600] adrenal gland disease
displayName
Defective CYP21A2 causes AH3
edited
[InstanceEdit:5579003] Jassal, Bijay, 2014年06月06日
eventOf
[Pathway:R-HSA-5579029] Metabolic disorders of biological oxidation enzymes - Homo sapiens
hasDiagram
true
hasEHLD
false
hasEvent
[FailedReaction:R-HSA-5601976] Defective CYP21A2 does not 21-hydroxylate PROG - Homo sapiens
isInDisease
true
isInferred
false
lastUpdatedDate
2019年03月25日
literatureReference
[LiteratureReference:5601952] Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
[LiteratureReference:5601979] Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood
maxDepth
2
modified
[InstanceEdit:9847082] Weiser, Joel, 2023年10月12日
name
Defective CYP21A2 causes AH3
Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
normalPathway
[Pathway:R-HSA-211945] Phase I - Functionalization of compounds
releaseDate
2014年12月11日
reviewStatus
[ReviewStatus:9821382] five stars
reviewed
[InstanceEdit:5634119] Nakaki, Toshio, 2014年11月03日
schemaClass
Pathway
species
[Species:48887] Homo sapiens
stId
R-HSA-5579021
summation
[Summation:5601945] Steroid 21-hydroxylase (CYP21A2) specifically catalyses the ...
updateTrackers
[UpdateTracker:9784928] Update Tracker - [Pathway:5579021] Defective CYP21A2 causes AH3 - v52:[removeHasEvent]
[UpdateTracker:9778344] Update Tracker - [Pathway:5579021] Defective CYP21A2 causes AH3 - v68:[updateContainedRLE]
Referrals
(updatedInstance)
[UpdateTracker:9784928] Update Tracker - [Pathway:5579021] Defective CYP21A2 causes AH3 - v52:[removeHasEvent]
[UpdateTracker:9778344] Update Tracker - [Pathway:5579021] Defective CYP21A2 causes AH3 - v68:[updateContainedRLE]
(hasEvent)
[Pathway:R-HSA-5579029] Metabolic disorders of biological oxidation enzymes
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