LHB, luteinizing hormone subunit beta, 3972

N. diseases: 62; N. variants: 11
Disease: Isolated lutropin deficiency (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		0.700 GeneticVariation disease UNIPROT Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. 1727547 1992
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		0.700 Biomarker disease CTD_human
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		0.700 CausalMutation disease CLINVAR
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		0.700 GermlineCausalMutation disease ORPHANET