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Term ID: | 14521 |
Name: | progressive myoclonic epilepsy type 7 |
Definition: | Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCNC1 gene. |
Alternative IDs: | 616187 |
ParentIDs: | |
TreeNumbers: | |
Synonyms: | epilepsy, progressive myoclonic 7; epilepsy, progressive myoclonic 7; EPM7; epilepsy, progressive myoclonic type 7; EPM7; KCNC1 progressive myoclonic epilepsy; meak; myoclonus epilepsy and ataxia due to potassium channel mutation; PME type 7; progressive myoclonic epilepsy caused by mutation in KCNC |
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Reference: |
MedGen:
MeSH:
OMIM: 616187; MSeqDR : Genes: KCNC1; | Could not execute query 3 SELECT t5.Variation_Name, t5.GeneID, t5.GeneSymbol, t5.ClinicalSignificance, t5.dbSNP, t5.RCVaccession, t5.TestedInGTR, t5.PhenotypeIDs, t5.Chromosome, t5.Start, t5.Stop, t5.HGVS_c, t5.HGVS_p, t5.HGVS_g, t5.OtherIDs, t5.Diseases as Disease_ClinVar
FROM gb_exome.clinvar_variation_v2_latest as t5
WHERE Assembly ='GRCh37' AND (t5.PhenotypeIDs like '%:616187%' OR t5.otherIDs like '%OMIM Allelic Variant:616187%' )
ORDER by GeneSymbol, t5.ClinicalSignificance LIKE 'Patho%' DESC, t5.ClinicalSignificance LIKE '%likely pathog%' DESC, start <1,start; |