Home > 2014 ICD-9-CM Diagnosis Codes > Congenital Anomalies 740-759 > Chromosomal anomalies 758-
Specific code 2014 ICD-9-CM Diagnosis Code 758.5
Other conditions due to autosomal anomalies
  • 2014
  • Billable Thru Sept 30/2015
  • Non-Billable On/After Oct 1/2015

  • Short description: Autosomal anomalies NEC.
  • ICD-9-CM 758.5 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.5 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 2014 version of ICD-9-CM 758.5.
  • More recent version(s) of ICD-9-CM 758.5: 2015.
Convert to ICD-10-CM: 758.5 converts approximately to:
  • 2015/16 ICD-10-CM Q92.8 Other specified trisomies and partial trisomies of autosomes
Approximate Synonyms
  • 10p partial trisomy syndrome
  • 10q partial trisomy syndrome
  • 11p partial trisomy syndrome
  • 11q partial trisomy syndrome
  • 12p partial trisomy syndrome
  • 12q partial trisomy syndrome
  • 15q partial trisomy syndrome
  • 16q partial trisomy syndrome
  • 17p partial trisomy syndrome
  • 17q partial trisomy syndrome
  • 19q partial trisomy syndrome
  • 1q partial trisomy syndrome
  • 20p partial trisomy syndrome
  • 20q partial trisomy syndrome
  • 2q partial trisomy syndrome
  • 3p partial trisomy syndrome
  • 3q partial trisomy syndrome
  • 4p partial trisomy syndrome
  • 4q partial trisomy syndrome
  • 5p partial trisomy syndrome
  • 6p partial trisomy syndrome
  • 6q partial trisomy syndrome
  • 7p partial trisomy syndrome
  • 7q partial trisomy syndrome
  • 8p partial trisomy syndrome
  • 8q partial trisomy syndrome
  • 9p partial trisomy syndrome
  • 9q partial trisomy syndrome
  • Autosomal aneuploidy
  • Autosomal anomaly
  • AUTOSOMAL ANOMALY (disorder)
  • Autosomal chromosomal disorder
  • Autosomal deletion - mosaicism
  • Autosomal dominant hereditary disorder
  • Autosomal duplication
  • Autosomal hereditary disorder
  • Autosomal recessive hereditary disorder
  • Complete trisomy 10 syndrome
  • Complete trisomy 20 syndrome
  • Complete trisomy 8 syndrome
  • Complete trisomy 9 syndrome
  • Dominant autosomal hereditary disorder, complete penetrance
  • Dominant autosomal hereditary disorder, incomplete penetrance
  • Individual with autosomal fragile site
  • Major partial trisomy
  • Partial trisomy syndromes
  • Pyle metaphyseal dysplasia
  • Trisomy 10
  • Trisomy 11
  • Trisomy 12
  • Trisomy 6
  • Trisomy 7
  • Trisomy 8
  • Trisomy 9
  • Trisomy and partial trisomy of autosome
  • Unbalanced translocation and insertion
  • Whole chromosome trisomy - meiotic nondisjunction
  • Whole chromosome trisomy - mitotic nondisjunction mosaicism
Applies To
  • Accessory autosomes NEC
ICD-9-CM Volume 2 Index entries containing back-references to 758.5:
 758.4 ICD9Data.com 758.6 
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 758.5 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 2014 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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