AVPR2, arginine vasopressin receptor 2, 554

N. diseases: 134; N. variants: 38
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0043116
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I
HMN (Hereditary Motor Neuropathy) Proximal Type I 		0.010 Biomarker disease BEFREE Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association. 671487 1978