CHI3L1, chitinase 3 like 1, 1116

N. diseases: 420; N. variants: 9
Disease: Hyperimmunoglobulin M syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272236
Disease: Hyperimmunoglobulin M syndrome
Hyperimmunoglobulin M syndrome 		0.010 GeneticVariation disease BEFREE These data suggest that a defect in gp39 is the basis of X-linked HIM. 7678782 1993