GLI2, GLI family zinc finger 2, 2736

N. diseases: 351; N. variants: 37
Disease: Pituitary dwarfism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		0.130 GeneticVariation disease BEFREE The primary aim of this study was to analyze the presence of GLI2 gene alterations in a cohort of patients with IGHD or MPHD and ectopic/absent posterior pituitary. 27576279 2017
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		0.130 Biomarker disease BEFREE The GLI2 coding region of 41 patients with severe isolated GH deficiency (IGHD) and 136 patients with CPHD was amplified by PCR using intronic primers and sequenced. 22967285 2013
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		0.130 Biomarker disease BEFREE The GLI2 coding region of patients with isolated GH deficiency (IGHD) or combined pituitary hormone deficiency was amplified by PCR using intronic primers and sequenced. 20685856 2010
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		0.130 Biomarker disease HPO