Disease #07148 (HH (hypogonadotropic hypogonadism))

Official abbreviation HH
Name hypogonadotropic hypogonadism
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TCF12
Associated tissues -
Disease features -
Remarks -
Date created 2025-01-23 09:27:10 +01:00 (CET)
Date last edited N/A


Individuals

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00464701 2192_Case9 - Pituitary insufficiency & diminished ovarian reserve, small uterus with septum F ? Canada French - - - - HH - HS6ST1 HS6ST1 1 1 Rima Slim
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