B2M, beta-2-microglobulin, 567

N. diseases: 352; N. variants: 6
Disease: Amyloidosis, familial visceral ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin. 22693999 2012
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin. 22693999 2012
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 GeneticVariation disease UNIPROT Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin. 22693999 2012
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 CausalMutation disease CLINVAR
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease CTD_human