1. Diseases
  2. DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect

DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect

Disease Export to PDF
Name:
DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect
ORPHAcode:
330050
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
DNM1L
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14