NIPBL, NIPBL cohesin loading factor, 25836

N. diseases: 169; N. variants: 268
Disease: Short stature ×
Source: INFERRED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0349588
Disease: Short stature
Short stature 		0.100 CausalMutation phenotype CLINVAR A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. 26938784 2016
CUI: C0349588
Disease: Short stature
Short stature 		0.100 Biomarker phenotype HPO