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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 759.0

Anomalies of spleen congenital

View the most recent version of ICD-9-CM 759.0

  • 759.0 is a specific code that can be used to specify a diagnosis
  • 759.0 contains 28 index entries
  • View the ICD-9-CM Volume 1 759.* hierarchy

Alternate Terminology

  • Aberrant spleen
  • Absent spleen
  • Accessory spleen
  • Congenital splenomegaly
  • Ectopic spleen
  • Lobulation of spleen


 Index entries containing 759.0:

Aberrant (congenital) - see also Malposition, congenital
  • spleen 759.0
    Absence (organ or part) (complete or partial)
    • spleen (congenital) 759.0
    Accessory (congenital)
    • spleen 759.0
      Agenesis - see also Absence, by site, congenital
      • spleen 759.0
        Anomaly, anomalous (congenital) (unspecified type) 759.9
        • specified type NEC
          • spleen 759.0
          • spleen 759.0
            Aplasia - see also Agenesis
            • spleen 759.0
              Asplenia 759.0Cyst (mucus) (retention) (serous) (simple)
              • spleen NEC 289.59
                • congenital 759.0
                Deformity 738.9
                • spleen
                  • congenital 759.0
                  Disease, diseased - see also Syndrome
                  • polycystic (congenital) 759.89
                    • spleen 759.0
                    • spleen (organic) (postinfectional) 289.50
                      • polycystic 759.0
                      Displacement, displaced
                      • spleen, congenital 759.0
                        Distortion (congenital)
                        • spleen 759.0
                          Ectopic, ectopia (congenital) 759.89
                          • spleen 759.0
                            Enlargement, enlarged - see also Hypertrophy
                            • spleen (see also Splenomegaly) 789.2
                              • congenital 759.0
                              Hypoplasia, hypoplasis 759.89
                              • spleen 759.0
                                Ivemark's syndrome (asplenia with congenital heart disease) 759.0
                                  Lobulation (congenital) - see also Anomaly, specified type NEC, by site
                                  • spleen 759.0
                                    Malposition
                                    • congenital
                                      • spleen 759.0
                                      Polycystic (congenital) (disease) 759.89
                                      • spleen 759.0
                                        Polysplenia syndrome 759.0
                                          Spleen, splenic - see also condition
                                          • agenesis 759.0
                                            Splenomegaly 789.2
                                            • congenital 759.0
                                              Supernumerary (congenital)
                                              • spleen 759.0
                                                Syndrome - see also Disease
                                                • Ivemark's (asplenia with congenital heart disease) 759.0
                                                  • polysplenia 759.0
                                                    • splenic
                                                      • agenesis 759.0