Symbol Name ID |
Acadm
acyl-Coenzyme A dehydrogenase, medium chain MGI:87867 |
Darker colors indicate more annotations |
Human Phenotypes | Distal arthrogryposis |
Hypotonia |
Generalized hypotonia |
Muscle spasm |
Fatigable weakness |
Fatigable weakness of neck muscles |
Proximal muscle weakness |
Skeletal muscle atrophy |
Myopathy |
Disease(s) Associated with ACADM | |||||||||
medium chain acyl-CoA dehydrogenase deficiency |
Mouse Phenotypes | abnormal myocardial fiber morphology |
myocardial fiber degeneration |
cardiomyopathy |
|
Availability | Mouse Genotype | |||
Acadmtm1Uab/Acadmtm1Uab |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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