SPTBN2, spectrin beta, non-erythrocytic 2, 6712

N. diseases: 79; N. variants: 11
Disease: Facial Myokymia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270871
Disease: Facial Myokymia
Facial Myokymia 		0.110 GeneticVariation phenotype BEFREE The authors present the first case of infantile-onset spinocerebellar ataxia associated with a novel SPTBN2 mutation (transition C>T at nucleotide position 1438), the proband having a much more severe phenotype with global developmental delay, hypotonia, tremor, nystagmus, and facial myokymia. 22914369 2013
CUI: C0270871
Disease: Facial Myokymia
Facial Myokymia 		0.110 Biomarker phenotype HPO