| Human Disease |
Cerebral Amyloid Angiopathy, Itm2b-Related, 1 OMIM ID: 176500 |
|||||||||||||||||||||
| Synonyms | Cerebral Amyloid Angiopathy, British Type; Dementia, Familial British; FBD; Presenile Dementia with Spastic Ataxia | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Itm2btm3.1Ldad/Itm2btm3.1Ldad |
B6.129-Itm2btm3.1Ldad | J:166696 | View |
| Itm2btm1.1Ldad/Itm2btm1.1Ldad |
involves: 129 | J:166696 | 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 05/22/2013 MGI 5.13 |
|
|
|
||