| Human Disease |
Growth Hormone Insensitivity with Immunodeficiency OMIM ID: 245590 |
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| Synonyms | Growth Hormone Insensitivity Due to Postreceptor Defect; Laron Syndrome Due to Postreceptor Defect | ||||||||||||||||||||||||||||
| 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 |
| Hnf1atm1.1Ylee/Hnf1atm1.1Ylee |
involves: 129X1/SvJ * C57BL/6J | J:47008 | 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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