Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 50
  • Symbol: ACO2
  • Description: aconitase 2

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Disease_Term Source Rank Other Values
?Optic atrophy 9, 616289 (3) OMIM high
  • Genome region : 22q13.2
  • OMIM_ID : 100850 OMIM gene ID
  • OMIM_ID : 616289 OMIM phenotype ID
Infantile cerebellar-retinal degeneration, 614559 (3) OMIM high
  • Genome region : 22q13.2
  • OMIM_ID : 100850 OMIM gene ID
  • OMIM_ID : 614559 OMIM phenotype ID