SGCE, sarcoglycan epsilon, 8910

N. diseases: 68; N. variants: 27
Disease: Benign Hereditary Chorea ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0393584
Disease: Benign Hereditary Chorea
Benign Hereditary Chorea 		0.010 Biomarker disease BEFREE Microdeletions of movement disorder genes including epsilon-sarcoglycan (SGCE) and thyroid transcription factor-1 (TITF1) have been described in patients with myoclonus dystonia and benign hereditary chorea respectively. 22515636 2012