MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Supranuclear Palsy, Progressive, 1, Atypical ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		0.710 GeneticVariation disease BEFREE Routine screening for MAPT mutations in atypical PSP is not recommended. 17274033 2007
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		0.710 SusceptibilityMutation disease ORPHANET
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		0.710 Biomarker disease CTD_human
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		0.710 CausalMutation disease CLINVAR