Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:84823
  • Symbol:LMNB2
  • Description:lamin B2

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Disease_Term Source Rank Other Values
{Lipodystrophy, partial, acquired, susceptibility to}, 608709 (3) OMIM high
  • Genome region :19p13.3
  • OMIM_ID :150341OMIM gene ID
  • OMIM_ID :608709OMIM phenotype ID
?Epilepsy, progressive myoclonic, 9, 616540 (3) OMIM high
  • Genome region :19p13.3
  • OMIM_ID :150341OMIM gene ID
  • OMIM_ID :616540OMIM phenotype ID