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
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 11 - 20 of 36 in total
HPO ID HPO Term
HP:0001608 Abnormality of the voice
HP:0000044 Hypogonadotropic hypogonadism
HP:0008187 Absence of secondary sex characteristics
HP:0000739 Anxiety
HP:0008734 Decreased testicular size
HP:0000823 Delayed puberty
HP:0000164 Abnormality of the dentition
HP:0003187 Breast hypoplasia
HP:0000002 Abnormality of body height
HP:0000939 Osteoporosis
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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