Disease #03011

Official abbreviation MC1DN-20
Name mitochondrial complex I deficiency, nuclear type 20 (MC1DN-20, acyl-CoA dehydrogenase family 9 deficiency)
OMIM ID 611126
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ACAD9
Associated tissues -
Disease features autosomal recessive
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00247793 - - - M - Russia - >00y01m 0 - - MC1DN-20 - - ACAD9 1 1 Valeriia Apukhtina
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