Disease #01388 (HH7 (hypogonadism, hypogonadotropic, type 7 (HH7)), OMIM:146110)

Official abbreviation HH7
Name hypogonadism, hypogonadotropic, type 7 (HH7)
OMIM ID 146110
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 5 genes FGFR1, FSHB, GNRH1, GNRHR, WDR11
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00103196 - - - - - Germany - - - - - HH7 - GNRHR GNRHR 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00385933 patient PubMed: Matthews 1993 - F - Italy - - - - - HH7 see paper; ..., primary amenorrhea, infertility, isolated deficiency pituitary FSH, normal LH FSHB FSHB 1 1 Johan den Dunnen
00385934 patient PubMed: Matthews 1997 2-generation family, 1 affected, unaffected heterozygous carrier relatives F - Israel Jewish-Europe - - - - HH7 primary amenorrhea, isolated FSH deficiency FSHB FSHB 1 1 Johan den Dunnen
00385935 patient PubMed: Layman 1997 3-generation family, 1 affected, unaffected heterozygous carrier parents F - United States - - - - - HH7 see paper; ..., delayed puberty, hypogonadism, FSH deficiency FSHB FSHB 2 1 Johan den Dunnen
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