| Human Disease |
Hyperparathyroidism, Neonatal Severe Primary; NSHPT OMIM ID: 239200 |
|||||||||||||||||||||
| Synonyms | NHPT; NSPH | |||||||||||||||||||||
| 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 |
| Casrtm1Ces/Casrtm1Ces |
involves: 129X1/SvJ * Black Swiss | J:29900 | 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 |
|
|
|
||