Home > 2010 ICD-9-CM Diagnosis Codes > Congential Anomalies 740-759 > Chromosomal anomalies 758-
Specific code 2010 ICD-9-CM Diagnosis Code 758.39
Other autosomal deletions
  • Short description: Autosomal deletions NEC.
  • ICD-9-CM 758.39 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.39 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2010 version of ICD-9-CM 758.39.
  • More recent version(s) of ICD-9-CM 758.39: 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: 758.39 converts approximately to:
  • 2015/16 ICD-10-CM Q93.3 Deletion of short arm of chromosome 4
    Or:
  • 2015/16 ICD-10-CM Q93.7 Deletions with other complex rearrangements
    Or:
  • 2015/16 ICD-10-CM Q93.89 Other deletions from the autosomes
Approximate Synonyms
  • 10p partial monosomy syndrome
  • 10q partial monosomy syndrome
  • 11p partial monosomy syndrome
  • 11q partial monosomy syndrome
  • 12p partial monosomy syndrome
  • 15q partial monosomy syndrome
  • 18q partial monosomy syndrome
  • 1p partial monosomy syndrome
  • 1q partial monosomy syndrome
  • 22q partial monosomy syndrome
  • 4p partial monosomy syndrome
  • 4q partial monosomy syndrome
  • 5p partial monosomy syndrome
  • 7p partial monosomy syndrome
  • 7q partial monosomy syndrome
  • 8p partial monosomy syndrome
  • 8q partial monosomy syndrome
  • 9p partial monosomy syndrome
  • 9q partial monosomy syndrome
  • Autosomal deletion syndrome
  • Complete monosomy 21 syndrome
  • Deletion of long arm of chromosome 13
  • Deletion of long arm of chromosome 18
  • Deletion of part of autosome
  • Deletion of short arm of chromosome 18
  • Deletion of X-chromosome and hypogammaglobulinemia
  • Deletion seen only at prometaphase
  • Deletion with complex rearrangement
  • Monosomy 22 and absence of immunoglobulin A
  • Monosomy and deletion from autosome
ICD-9-CM Volume 2 Index entries containing back-references to 758.39:
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
  • 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
    • chromosome 4 short arm deletion 758.39
    • deletion chromosomes 758.39
    • long arm 18 or 21 deletion 758.39
 758.33 ICD9Data.com 758.4 
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 758.39 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2010 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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