Gene: FXN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2395
Gene Symbol: FXN
FXN 		0.110 Biomarker phenotype BEFREE The presence of spasticity and pyramidal features is a hallmark of some of hereditary ataxias, such as autosomal-recessive spastic ataxia of Charlevoix-Saguenay, other primary spastic ataxias, Friedreich ataxia, or ataxia with isolated vitamin E deficiency. 29891058 2018
Entrez Id: 2395
Gene Symbol: FXN
FXN 		0.110 Biomarker phenotype HPO