STMN1, stathmin 1, 3925

N. diseases: 284; N. variants: 1
Disease: Childhood Anaplastic Oligodendroglioma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1332943
Disease: Childhood Anaplastic Oligodendroglioma
Childhood Anaplastic Oligodendroglioma 		0.010 GeneticVariation disease BEFREE Loss of heterozygosity for the stathmin gene may be associated with improved outcomes of patients with 1p+/- anaplastic oligodendroglioma tumors. 17440165 2007