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