| Human Disease |
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy; OMIM ID: 221770 |
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| Synonyms | Brain-Bone-Fat Disease; Dementia, Prefrontal, with Bone Cysts; Dementia, Progressive, with Lipomembranous Polycystic Osteodysplasia; Nasu-Hakola Disease; NHD; Plosl; Presenile Dementia with Bone Cysts | ||||||||||||||||||||||||||||
| 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 |
| Tyrobptm1Ttk/Tyrobptm1Ttk |
involves: 129P2/OlaHsd * C57BL/6 | J:81823 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tyrobptm1.1Viv/Tyrobptm1.1Viv |
B6.129P2-Tyrobptm1.1Viv | J:95232 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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