IGHD, immunoglobulin heavy constant delta, 3495

N. diseases: 21; N. variants: 0
Disease: Isolated somatotropin deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		0.020 GeneticVariation disease BEFREE Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD. 26612202 2016
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		0.020 GeneticVariation disease BEFREE Catch-up growth in autosomal dominant isolated growth hormone deficiency (IGHD type II). 17360215 2007