Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9394
Gene Symbol: HS6ST1
HS6ST1
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.300 GermlineCausalMutation ORPHANET Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes. 23997646

2013
Entrez Id: 9394
Gene Symbol: HS6ST1
HS6ST1
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.300 GermlineCausalMutation ORPHANET Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism. 21700882

2011