Disease #05235 (EMPF2 (encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission, type 2 (EMPF-2)), OMIM:617086)

Global Variome shared LOVD

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Official abbreviation	EMPF2
Name	encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission, type 2 (EMPF-2)
OMIM ID	617086
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MFF
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-03-09 23:07:29 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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