| Human Disease |
Hypogonadotropic Hypogonadism 1 with or without Anosmia; HH1 OMIM ID: 308700 |
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| Synonyms | Anosmic Hypogonadism; Dysplasia Olfactogenitalis of De Morsier; Hypogonadotropic Hypogonadism and Anosmia; HHA; Kallmann Syndrome 1; KAL1; KMS | |||||||||||||||||||||
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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 06/12/2013 MGI 5.14 |
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