Disease: Dystrophia unguium ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		0.110 GeneticVariation disease BEFREE Mutations in ATP6V1B2, which encodes the B2 subunit of the vacuolar H + ATPase have previously been associated with Zimmermann-Laband syndrome 2 (ZLS2) and deafness-onychodystrophy (DDOD) syndrome. 31655144 2019
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		0.110 Biomarker disease HPO