Disease #03011 (MC1DN20 (mitochondrial complex I deficiency, nuclear type 20 (MC1DN20, acyl-CoA dehydrogenase family 9 deficiency)), OMIM:611126)

Official abbreviation MC1DN20
Name mitochondrial complex I deficiency, nuclear type 20 (MC1DN20, acyl-CoA dehydrogenase family 9 deficiency)
OMIM ID 611126
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ACAD9
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-19 07:44:35 +02:00 (CEST)


Individuals

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00247793 - - - M - Russia - >00y01m - - - MC1DN20 - - ACAD9 1 1 Valeriia Apukhtina
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