| Human Disease |
Thrombotic Thrombocytopenic Purpura, Congenital; TTP OMIM ID: 274150 |
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| Synonyms | Microangiopathic Hemolytic Anemia; Microangiopathic Hemolytic Anemia, Congenital; Schulman-Upshaw Syndrome; Thrombotic Microangiopathy, Familial; Thrombotic Thrombocytopenic Purpura, Familial; Upshaw Factor, Deficiency of; Upshaw-Schulman Syndrome; USS | |||||||||||||||||||||
| 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 |
| Adamts13tm1Dgi/Adamts13tm1Dgi |
involves: 129X1/SvJ * C57BL/6J * CASA/Rk | J:101752 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Adamts13tm1Myta/Adamts13tm1Myta |
involves: 129S6/SvEvTac | J:125786 | View |
| Adamts13tm1Dgi/Adamts13tm1Dgi |
involves: 129X1/SvJ * C57BL/6J | J:101752 | 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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