generalized epilepsy-paroxysmal dyskinesia syndrome
gene (chromosome 10q22), encoding the alpha subunit of the BK channel. Transmission is autosomal dominant.
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generalized epilepsy-paroxysmal dyskinesia syndrome
Summary
generalized epilepsy-paroxysmal dyskinesia syndrome is a rare disease[1].
Key Facts
- generalized epilepsy-paroxysmal dyskinesia syndrome's instance of is recorded as rare disease[2].
- generalized epilepsy-paroxysmal dyskinesia syndrome's instance of is recorded as class of disease[3].
- generalized epilepsy-paroxysmal dyskinesia syndrome's subclass of is recorded as familial partial epilepsy[4].
- generalized epilepsy-paroxysmal dyskinesia syndrome's MeSH descriptor ID is recorded as C563719[5].
- generalized epilepsy-paroxysmal dyskinesia syndrome's OMIM ID is recorded as 609446[6].
- generalized epilepsy-paroxysmal dyskinesia syndrome's KEGG ID is recorded as H01258[7].
- generalized epilepsy-paroxysmal dyskinesia syndrome's Orphanet ID is recorded as 79137[8].
- generalized epilepsy-paroxysmal dyskinesia syndrome's genetic association is recorded as KCNMA1[9].
- generalized epilepsy-paroxysmal dyskinesia syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79137[10].
- generalized epilepsy-paroxysmal dyskinesia syndrome's UMLS CUI is recorded as C1836173[11].
- generalized epilepsy-paroxysmal dyskinesia syndrome's ICD-10-CM is recorded as G40.3[12].
- generalized epilepsy-paroxysmal dyskinesia syndrome's Mondo ID is recorded as MONDO_0012276[13].