| Human Disease |
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of; ACADSD OMIM ID: 201470 |
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| Synonyms | ACADS Deficiency; Lipid-Storage Myopathy Secondary to Short-Chain Acyl-CoA Dehydrogenase Deficiency; Scad Deficiency; Scadh Deficiency | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Acadsdel-J/Acadsdel-J |
BALB/cByJ | J:9743 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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