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2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Certain Congenital Musculoskeletal Deformities 754.* >

2006 ICD-9-CM Diagnosis 754.89

Other specified nonteratogenic anomalies

View the most recent version of ICD-9-CM 754.89

  • 754.89 is a specific code that can be used to specify a diagnosis
  • 754.89 contains 16 index entries
  • View the ICD-9-CM Volume 1 754.* hierarchy

Alternate Terminology

  • Club hand (congenital)
  • Congenital:
    • deformity of chest wall
    • dislocation of elbow
  • Generalized flexion contractures of lower limb joints, congenital
  • Spade-like hand (congenital)


 Index entries containing 754.89:

Anomaly, anomalous (congenital) (unspecified type) 759.9
  • joint 755.9
    • multiple arthrogryposis 754.89
    • nonteratogenic NEC 754.89
      Arthrogryposis 728.3
      • multiplex, congenita 754.89
        Clubfinger 736.29
        • congenital 754.89
          Club hand (congenital) 754.89Contraction, contracture, contracted
          • joint (abduction) (acquired) (adduction) (flexion) (rotation) 718.40
            • congenital NEC 755.8
              • generalized or multiple 754.89
                • lower limb joints 754.89
                • lower limb (including pelvic girdle) not involving hip 754.89
              Deformity 738.9
              • chest (wall) (acquired) 738.3
                • congenital 754.89
                • thorax (acquired) (wall) 738.3
                  • congenital 754.89
                  Dislocation (articulation) (closed) (displacement) (simple) (subluxation) 839.8
                  • elbow (closed) 832.00
                    • congenital 754.89
                    Flat
                    • chest, congenital 754.89
                      Guérin-Stern syndrome (arthrogryposis multiplex congenita) 754.89
                        Rigid, rigidity - see also condition
                        • articular, multiple congenital 754.89
                          Spade-like hand (congenital) 754.89
                            Syndrome - see also Disease
                            • Guérin-Stern (arthrogryposis multiplex congenita) 754.89