IGHD, immunoglobulin heavy constant delta, 3495

N. diseases: 21; N. variants: 0
Disease: Laron Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271568
Disease: Laron Syndrome
Laron Syndrome 		0.010 Biomarker disease BEFREE Only patients with an ascertained diagnosis of either Laron syndrome (LS), congenital IGHD, congenital multiple pituitary hormone deficiency (cMPHD) including GH or GHRHR defect were included in this study. 21292919 2011