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Congenital Adrenal Hyperplasia

Disease ID: disease_node_16839

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Dbxref	GARD:1465, GARD:1467, ICD10CM:E25, ICD9CM:255.2, MIM:201710, MIM:201810, MIM:201910, MIM:202010, MIM:202110, ORDO:418, SNOMEDCT_US_2023_03_01:154706003, UMLS_CUI:C0701163
Subclassof	DOID_0080015, DOID_1701
Data Source	DOID
Synonyms	adrenal hyperplasia 1, congenital lipoid adrenal hyperplasia, lipoid CAH
Doid Label	congenital adrenal hyperplasia
Doid Description	A steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgyny manifestations resulting from steroidogenic enzyme deficiency. Xref MGI.
Disease Node Id	disease_node_16839
Doid Id	DOID_0050811
Disease Has Basis In	HP_0001197
Label	Congenital Adrenal Hyperplasia

Outgoing r'ship SUBCLASS_OF to/from Steroid Metabolism, Inborn Errors(ID:disease_node_11191) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Physical Disorder(ID:disease_node_13159) (Disease)

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