| Human Disease |
Hyperinsulinemic Hypoglycemia, Familial, 2; HHF2 OMIM ID: 601820 |
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| Synonyms | Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia; Hyperinsulinemic Hypoglycemia, Persistent; Hyperinsulinism, Congenital; Hyperinsulinism, Familial; Hyperinsulinism, Neonatal; Nesidioblastosis; Persistent Hyperinsulinemic Hypoglycemia of Infancy; PHHI | ||||||||||||||||||||||||||||
| 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 |
| Abcc8tm1.1Mgn/Abcc8tm1.1Mgn |
involves: 129X1/SvJ * C57BL/6 | J:79352 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Abcc8tm1Jbry/Abcc8tm1Jbry |
involves: 129X1/SvJ * C57BL/6 | J:61356 | 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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