NEFH, neurofilament heavy, 4744

N. diseases: 120; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal
0.200 Biomarker disease RGD Retarded development of neurons and oligodendroglia in rat forebrain produced by hyperphenylalaninemia results in permanent deficits in myelin despite long recovery periods. 7507064 1993