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2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Other And Unspecified Congenital Anomalies 759.* >

2006 ICD-9-CM Diagnosis 759.82

Marfan syndrome

View the most recent version of ICD-9-CM 759.82

  • A hereditary disorder of connective tissue characterized by tall stature, elongated extremities, subluxation of the lens, dilatation of the ascending aorta, and "pigeon breast." It is inherited as an autosomal dominant trait.
  • 759.82 is a specific code that can be used to specify a diagnosis
  • 759.82 contains 10 index entries
  • View the ICD-9-CM Volume 1 759.* hierarchy

 Index entries containing 759.82:

Acrochondrohyperplasia 759.82
    Arachnodactyly 759.82
      Beals syndrome 759.82
        Disease, diseased - see also Syndrome
        • Marfan's 090.49
          • meaning Marfan's syndrome 759.82
          Dolichostenomelia 759.82
            Dysmorodystrophia mesodermalis congenita 759.82
              Dystrophy, dystrophia 783.9
              • mesodermalis congenita 759.82
                Marfan's
                • syndrome (arachnodactyly) 759.82
                Syndrome - see also Disease
                • Beals 759.82
                  • Marfan's (arachnodactyly) 759.82