TCN2, transcobalamin 2, 6948

N. diseases: 104; N. variants: 30
Disease: Childhood Ataxia with Central Nervous System Hypomyelinization ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1858991
Disease: Childhood Ataxia with Central Nervous System Hypomyelinization
Childhood Ataxia with Central Nervous System Hypomyelinization 		0.300 Biomarker disease CTD_human MTX-induced white matter changes are associated with polymorphisms of methionine metabolism. 15753437 2005