All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01388 HH7 hypogonadism, hypogonadotropic, type 7 (HH7) 146110 AR 4 4 FGFR1, FSHB, GNRH1, GNRHR, WDR11 - -
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