Disease #01388

Official abbreviation HH
Name hypogonadism, hypogonadotropic (HH)
OMIM ID 146110
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes GNRH1, GNRHR
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00103196 - - - - - Germany - - 0 - - HH - GNRHR GNRHR 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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