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DOID:0090078 - hypogonadotropic hypogonadism 7 with or without anosmia
Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported.
Synonyms:
| OMIM:146110 - HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7 |
| MONDO:0007794 - hypogonadotropic hypogonadism 7 with or without anosmia |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes
:
spry4,
il17rd,
flrt3,
prok2,
axl,
sema3e,
gnrh1,
dusp6,
fezf1,
kiss1r,
wdr11,
sra1,
nsmf,
gnrhr,
polr3b,
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
hypogonadotropic hypogonadism (is_a)