2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Chromosomal Anomalies 758.* > 2006 ICD-9-CM Diagnosis 758.39 Other autosomal deletions View the most recent version of ICD-9-CM 758.39 758.39 is a specific code that can be used to specify a diagnosis 758.39 contains 9 index entries View the ICD-9-CM Volume 1 758.* hierarchy  Index entries containing 758.39: Anomaly, anomalous (congenital) (unspecified type) 759.9 chromosomes, chromosomal 758.9 autosomes NEC (see also Abnormal, autosomes) 758.5 deletion 758.39 Christchurch 758.39 Antimongolism syndrome 758.39 Deletion syndrome autosomal NEC 758.39 constitutional 5q deletion 758.39 Syndrome - see also Disease antimongolism 758.39 autosomal - see also Abnormal, autosomes NEC deletion 758.39 5p 758.31 22q11.2 758.32 with acute bronchitis 491.22 exacerbation (acute) 491.21 chromosome 4 short arm deletion 758.39 deletion chromosomes 758.39 long arm 18 or 21 deletion 758.39