Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 GeneticVariation disease BEFREE EAST (Epilepsy, Ataxia, Sensorineural deafness, Tubulopathy) or SeSAME (Seizures, Sensorineural deafness, Ataxia, Mental retardation, and Electrolyte imbalance) syndrome is a rare autosomal recessive syndrome first described in 2009 independently by Bockenhauer and Scholl. 29722015 2019
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 CausalMutation disease CLINVAR
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker disease MGD KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential. 11788352 2002
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 GeneticVariation disease BEFREE The present cases harboring novel homozygous frameshift mutations in KCNJ10 expand the spectrum of brain abnormalities in EAST syndrome, including mild cerebellar atrophy and intramyelinic edema, resulting from abnormal function of the Kir4.1 inwardly rectifying potassium channel at the astrocyte endfeet, with disruption of water-ion homeostasis. 29666984 2018
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 GeneticVariation disease UNIPROT Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10. 19289823 2009
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker disease BEFREE To better understand the role of the inward-rectifying K channel Kir4.1 (KCNJ10) in the distal nephron, we initially studied a global Kir4.1 knockout mouse (gKO), which demonstrated the hypokalemia and hypomagnesemia seen in SeSAME/EAST syndrome and was associated with reduced Na/Cl cotransporter (NCC) expression. 30110571 2018
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker disease CTD_human
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 GeneticVariation disease UNIPROT Mutations in KCNJ10 cause a specific disorder, consisting of epilepsy, ataxia, sensorineural deafness, and tubulopathy. 19420365 2009
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker disease GENOMICS_ENGLAND Patients clinically diagnosed with EAST syndrome were genotyped to identify and study mutations in KCNJ10. 21849804 2011