Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 57468
  • Symbol: SLC12A5
  • Description: solute carrier family 12 member 5

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Disease_Term Source Rank Other Values
Epileptic encephalopathy, early infantile, 34, 616645 (3) OMIM high
  • Genome region : 20q13.12
  • OMIM_ID : 606726 OMIM gene ID
  • OMIM_ID : 616645 OMIM phenotype ID
{Epilepsy, idiopathic generalized, susceptibility to, 14}, 616685 (3) OMIM high
  • Genome region : 20q13.12
  • OMIM_ID : 606726 OMIM gene ID
  • OMIM_ID : 616685 OMIM phenotype ID