IFT172, intraflagellar transport 172, 26160

N. diseases: 123; N. variants: 31
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 A case of functional growth hormone deficiency and early growth retardation in a child with IFT172 mutations. 25664603 2015