Gene: APTX ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54840
Gene Symbol: APTX
APTX 		0.110 Biomarker disease BEFREE Ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome [AOA]; MIM 208920) is an autosomal recessive disorder characterized by ataxia, oculomotor apraxia, and choreoathetosis. 11022012 2000
Entrez Id: 54840
Gene Symbol: APTX
APTX 		0.110 Biomarker disease HPO