AVPR1A, arginine vasopressin receptor 1A, 552

N. diseases: 51; N. variants: 9
Disease: Congenital adrenal hyperplasia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		0.300 Biomarker disease CTD_human Familial adrenocorticotropin-independent macronodular adrenal hyperplasia with aberrant serotonin and vasopressin adrenal receptors. 17218722 2007