HGH1, HGH1 homolog, 51236

N. diseases: 6; N. variants: 0
Disease: Somatotropin deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		0.010 GeneticVariation disease BEFREE These data are important for prenatal diagnosis of at-risk pregnancies and for families at risk for recurrence and underline clearly the fact that the hGH-I gene deletion represents a common cause for growth hormone deficiency associated with severe growth retardation (height less than -4.5 SD score). 1603635 1992