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

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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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	-
Phenotype entries for this disease	-
Associated with 1 gene	DNM1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-01-21 21:26:45 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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