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Summary Literature (0)
MIM:614388 - ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1; EMPF1

Xenbase Genes: dnm1l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013726 - encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1

Disease Ontology (DO):
DOID:0070347 - encephalopathy due to defective mitochondrial and peroxisomal fission 1