TMEM106B, transmembrane protein 106B, 54664

N. diseases: 126; N. variants: 13
Disease: Leukodystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		0.110 GeneticVariation disease BEFREE A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy. 29186371 2017
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		0.110 Biomarker disease HPO