Disease #05550 (EMPF1 (encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF-1)), OMIM:614388)

Official abbreviation EMPF1
Name encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF-1)
OMIM ID 614388
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DNM1L
Associated tissues -
Disease features -
Remarks -