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 -
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.