| Human Disease |
Dopamine Beta-Hydroxylase Deficiency, Congenital OMIM ID: 223360 |
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| Synonyms | Noradrenaline Deficiency; Norepinephrine Deficiency | |||||||||||||||||||||
| 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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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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