| Human Disease |
Chanarin-Dorfman Syndrome; CDS OMIM ID: 275630 |
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| Synonyms | Chanarin-Dorfman Disease; Dorfman-Chanarin Syndrome; DCS; Ichthyosiform Erythroderma with Leukocyte Vacuolation; Ichthyotic Neutral Lipid Storage Disease; Neutral Lipid Storage Disease with Ichthyosis; NLSDI; Triglyceride Storage Disease with Impaired Long-Chain Fatty Acid Oxidation | |||||||||||||||||||||
| 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 |
| Abhd5tm1.1Rze/Abhd5tm1.1Rze |
involves: 129P2/OlaHsd * C57BL/6 | J:160725 | 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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