- clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material, either a whole chromosome or a chromosome segment.
758 Chromosomal anomalies convert 758 to ICD-10
758.0 Down's syndrome convert 758.0 to ICD-10
758.1 Patau's syndrome convert 758.1 to ICD-10
758.2 Edwards' syndrome convert 758.2 to ICD-10
758.3 Autosomal deletion syndromes convert 758.3 to ICD-10

758.31 Cri-du-chat syndrome convert 758.31 to ICD-10

758.32 Velo-cardio-facial syndrome convert 758.32 to ICD-10

758.33 Other microdeletions convert 758.33 to ICD-10

758.39 Other autosomal deletions convert 758.39 to ICD-10
758.4 Balanced autosomal translocation in normal individual convert 758.4 to ICD-10
758.5 Other conditions due to autosomal anomalies convert 758.5 to ICD-10
758.6 Gonadal dysgenesis convert 758.6 to ICD-10
758.7 Klinefelter's syndrome convert 758.7 to ICD-10
758.8 Other conditions due to chromosome anomalies convert 758.8 to ICD-10

758.81 Other conditions due to sex chromosome anomalies convert 758.81 to ICD-10

758.89 Other conditions due to chromosome anomalies convert 758.89 to ICD-10
758.9 Conditions due to anomaly of unspecified chromosome convert 758.9 to ICD-10