CSTB, cystatin B, 1476

N. diseases: 155; N. variants: 14
Disease: Apraxia, oculomotor, Cogan type ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0543874
Disease: Apraxia, oculomotor, Cogan type
Apraxia, oculomotor, Cogan type 		0.010 GeneticVariation disease BEFREE We report three new clinical features of ULD; ocular motor apraxia, dystonia, and rapidly progressive dementia. 17994572 2008