Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 4627
  • Symbol: MYH9
  • Description: myosin heavy chain 9

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Disease_Term Source Rank Other Values
May-Hegglin anomaly, 155100 (3) OMIM high
  • Genome region : 22q12.3
  • OMIM_ID : 155100 OMIM phenotype ID
  • OMIM_ID : 160775 OMIM gene ID
Deafness, autosomal dominant 17, 603622 (3) OMIM high
  • Genome region : 22q12.3
  • OMIM_ID : 160775 OMIM gene ID
  • OMIM_ID : 603622 OMIM phenotype ID
Fechtner syndrome, 153640 (3) OMIM high
  • Genome region : 22q12.3
  • OMIM_ID : 153640 OMIM phenotype ID
  • OMIM_ID : 160775 OMIM gene ID
Sebastian syndrome, 605249 (3) OMIM high
  • Genome region : 22q12.3
  • OMIM_ID : 160775 OMIM gene ID
  • OMIM_ID : 605249 OMIM phenotype ID
Macrothrombocytopenia and progressive sensorineural deafness, 600208 (3) OMIM high
  • Genome region : 22q12.3
  • OMIM_ID : 160775 OMIM gene ID
  • OMIM_ID : 600208 OMIM phenotype ID
Epstein syndrome, 153650 (3) OMIM high
  • Genome region : 22q12.3
  • OMIM_ID : 153650 OMIM phenotype ID
  • OMIM_ID : 160775 OMIM gene ID
Optic nerve measurement (rim area) GWAS high
Diabetic kidney disease GWAS high
Glomerulosclerosis GWAS high
End-stage renal disease (non-diabetic) GWAS high