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Congenital primary adrenocortical hypofunction

MedGen UID:
78784
•Concept ID:
C0271740
•
Disease or Syndrome
Synonyms: ADDISON DISEASE, CONGENITAL; Adrenocortical hypofunction, chronic primary congenital
SNOMED CT: Congenital primary adrenocortical hypofunction (12427005); Congenital Addison disease (12427005)
 
Monarch Initiative: MONDO:0007071
OMIM®: 103230

Recent clinical studies

Diagnosis

Autoimmune Addison's disease.
Betterle C, Morlin L
Endocr Dev 2011;20:161-172. Epub 2010 Dec 16 doi: 10.1159/000321239. PMID: 21164269
Diseases of the adrenal cortex.
Kannan CR
Dis Mon 1988 Oct;34(10):601-74. doi: 10.1016/0011-5029(88)90023-5. PMID: 3053076

Therapy

Autoimmune Addison's disease.
Betterle C, Morlin L
Endocr Dev 2011;20:161-172. Epub 2010 Dec 16 doi: 10.1159/000321239. PMID: 21164269

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