Disease #00587

Official abbreviation 618232
Name MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9
OMIM ID 618232
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFS6
Associated tissues -
Disease features -
Remarks -

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