MFF, mitochondrial fission factor, 56947

N. diseases: 44; N. variants: 7
Disease: Seizures ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures 		0.110 GeneticVariation phenotype BEFREE We suggest that, even if laboratory findings are not indicative of mitochondrial or peroxisomal dysfunction, the co-occurrence of optic and/or peripheral neuropathy with seizures warrants genetic testing for MFF mutations. 26783368 2016
CUI: C0036572
Disease: Seizures
Seizures 		0.110 Biomarker phenotype HPO