Disease: Kallmann Syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1563719
Disease: Kallmann Syndrome 1
Kallmann Syndrome 1 		0.100 CausalMutation disease CLINVAR When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR). 22745237 2012