| Human Disease |
Pituitary Hormone Deficiency, Combined, 3; CPHD3 OMIM ID: 221750 |
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| Synonyms | Deafness, Sensorineural, with Pituitary Dwarfism; Pituitary Hormone Deficiency, Combined, with Rigid Cervical Spine | |||||||||||||||||||||
| 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 |
| Lhx3tm1.1Sjr/Lhx3tm1.1Sjr |
involves: 129S/SvEv * C57BL/6J * FVB/N | J:169035 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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