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 11 - 20 of 25 in total
Gene ID Gene Symbol Description Source
2619 GAS1 growth arrest specific 1
2710 GK glycerol kinase
2817 GPC1 glypican 1
3293 HSD17B3 hydroxysteroid 17-beta dehydrogenase 3
3897 L1CAM L1 cell adhesion molecule
4594 MMUT methylmalonyl-CoA mutase
4907 NT5E 5'-nucleotidase ecto
5373 PMM2 phosphomannomutase 2
6296 ACSM3 acyl-CoA synthetase medium chain family member 3
6646 SOAT1 sterol O-acyltransferase 1
Related Glycoprotein
Displaying entry 21 - 21 of 21 in total
UniProt ID Protein Name Source
Q8IY17 Patatin-like phospholipase domain-containing protein 6
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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