| Human Disease |
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of; ACADMD OMIM ID: 201450 |
|||||||||||||||||||||
| Synonyms | ACADM Deficiency; Carnitine Deficiency Secondary to Medium-Chain Acyl-Coa Dehydrogenase Deficiency; MCAD Deficiency; MCADH Deficiency | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Acadmtm1Uab/Acadmtm1Uab |
involves: 129P2/OlaHsd * C57BL/6 | J:115759 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 06/05/2013 MGI 5.13 |
|
|
|
||