MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 324; N. variants: 57
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic
0.010 GeneticVariation phenotype BEFREE Autonomic dysfunction in mental retardation and spastic paraparesis with MECP2 mutation. 15704871 2004