hypogonadotropic hypogonadism 7 with or without anosmia

Summary
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.
Super Class
autosomal recessive disease hypogonadotropic hypogonadism
Related Genes
Displaying entries 21 - 25 of 25 in total
Gene ID Gene Symbol Description Source
8482 SEMA7A semaphorin 7A (JohnMiltonHagen blood group)
9394 HS6ST1 heparan sulfate 6-O-sulfotransferase 1
10908 PNPLA6 patatin like phospholipase domain containing 6
55512 SMPD3 sphingomyelin phosphodiesterase 3
148738 HJV hemojuvelin BMP co-receptor
The Human Phenotype Ontology
Displaying entries 31 - 36 of 36 in total
HPO ID HPO Term
HP:0000054 Micropenis
HP:0002231 Sparse body hair
HP:0000026 Male hypogonadism
HP:0000869 Secondary amenorrhea
HP:0003782 Eunuchoid habitus
HP:0000175 Cleft palate
Displaying 1 entry
Gene ID Gene Symbol Description
9394 HS6ST1 heparan sulfate 6-O-sulfotransferase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024