Disease: Deafness, Sensorineural, Autosomal-Mitochondrial Type ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1857332
Disease: Deafness, Sensorineural, Autosomal-Mitochondrial Type
Deafness, Sensorineural, Autosomal-Mitochondrial Type 		0.300 GermlineModifyingMutation phenotype ORPHANET Nuclear factors: roles related to mitochondrial deafness. 23510774 2013