F13B, coagulation factor XIII B chain, 2165

N. diseases: 47; N. variants: 23
Disease: Hereditary Factor XIII Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency 		0.600 GermlineCausalMutation disease ORPHANET Novel aspects of factor XIII deficiency. 21738029 2011
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency 		0.600 Biomarker disease CTD_human A familial factor XIII subunit B deficiency. 2334637 1990
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency 		0.600 Biomarker disease GENOMICS_ENGLAND