Disease #06673 (MC1DN13 (?Mi complex I deficiency, nuclear type 13), OMIM:618235)

Official abbreviation MC1DN13
Name ?Mi complex I deficiency, nuclear type 13
OMIM ID 618235
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NDUFA2
Associated tissues -
Disease features -
Remarks -