Disease #00582

Official abbreviation 618225
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4
OMIM ID 618225
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFV1
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 21
LOVD software ©2004-2018 Leiden University Medical Center