All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01519 CPPB1 puberty, precocious, central, type 1 (CPPB1) 176400 AD - - KISS1R - -
03747 HH13 hypogonadism, hypogonadotropic, type 13 with/without anosmia (HH-13) 614842 AR - - KISS1 - -
03742 HH8 hypogonadism, hypogonadotropic, type 8 with/without anosmia (HH-8) 614837 AR 1 - KISS1R - -
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