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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|