POU3F4, POU class 3 homeobox 4, 5456

N. diseases: 65; N. variants: 18
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 GermlineCausalMutation phenotype ORPHANET Phenotype and genotype in females with POU3F4 mutations. 19930154 2009