FMR1-IT1, FMR1 intronic transcript 1, 106478973

N. diseases: 29; N. variants: 0
Disease: Cerebral dysfunction ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction 		0.010 GeneticVariation disease BEFREE Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability. 7585014 1995