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Results for Proteins associated with the Gene: MYH9
MYH9
4627


Known Diseases associated with this Protein:
  ALPORT SYNDROME, WITH MACROTHROMBOCYTOPENIA (APSM)
  DEAFNESS, AUTOSOMAL DOMINANT 17
  DEAFNESS, AUTOSOMAL DOMINANT, 17 (DFNA17)
  EPSTEIN SYNDROME
  EPSTEIN SYNDROME (EPS)
  EPSTEIN SYNDROME, INCLUDED
  EPSTEIN SYNDROME, INCLUDED;;
  FECHTNER SYNDROME
  FECHTNER SYNDROME (FTNS)
  FECHTNER SYNDROME, INCLUDED
  FECHTNER SYNDROME, INCLUDED;;
  MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS, INCLUD
  MAY-HEGGLIN ANOMALY
  MAY-HEGGLIN ANOMALY (MHA)
  MAY-HEGGLIN ANOMALY, INCLUDED
  SEBASTIAN SYNDROME
  SEBASTIAN SYNDROME (SBS)
  SEBASTIAN SYNDROME, INCLUDED
  SEBASTIAN SYNDROME, INCLUDED;;
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 The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model.
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