Human Disease and Mouse Model Detail
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Human Disease
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Isolated Growth Hormone Deficiency, Type III; IGHD3
OMIM ID: 307200
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Synonyms
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Agammaglobulinemia and Isolated Growth Hormone Deficiency, X-Linked;
Fleisher Syndrome;
Growth Hormone Deficiency with Hypogammaglobulinemia;
Hypogammaglobulinemia and Isolated Growth Hormone Deficiency, X-Linked;
IGHD III
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Btk
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BTK*
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1:1 Homology
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Analysis Tools