The annotation has been inferred from sequence or structural similarity with Scn4a (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
Curation Notes: ClinVar Annotator: match by term: Familial hyperkalemic periodic paralysis | ClinVar Annotator: match by term: Gamstorp disease | ClinVar Annotator: match by term: Hyperkalemic periodic paralysis | ClinVar Annotator: match by term: SODIUM CHANNEL MUSCLE DISEASE
Curation Notes: ClinVar Annotator: match by term: Familial hyperkalemic periodic paralysis | ClinVar Annotator: match by term: Gamstorp disease | ClinVar Annotator: match by term: Hyperkalemic periodic paralysis
Curation Notes: ClinVar Annotator: match by term: Familial hyperkalemic periodic paralysis | ClinVar Annotator: match by term: Gamstorp disease | ClinVar Annotator: match by term: Hyperkalemic periodic paralysis
Curation Notes: ClinVar Annotator: match by term: Familial hyperkalemic periodic paralysis | ClinVar Annotator: match by term: Gamstorp disease | ClinVar Annotator: match by term: Hyperkalemic periodic paralysis
Curation Notes: ClinVar Annotator: match by term: Hyperkalemic periodic paralysis | ClinVar Annotator: match by term: Paramyotonia congenita/hyperkalemic periodic paralysis
An association has been curated linking SCN4A
and hyperkalemic periodic paralysis in Homo sapiens.
The association was inferred by association of genotype and phenotype (IAGP)