758.39 AUTOSOMAL DELETIONS NEC


Code Information

Diagnosis Code: 758.39

Short Description: Autosomal deletions NEC

Long Description: Other autosomal deletions

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 758 Chromosomal anomalies
        • 758.39 Autosomal deletions NEC

Code Version: 2015 ICD-9-CM


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
  • 22q13.3 deletion 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
  • Chromosome 11p11.2 deletion syndrome
  • Chromosome 16p11.2 deletion syndrome
  • Chromosome 1p36 deletion syndrome
  • Chromosome 2q37 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
  • Sensorineural deafness and male infertility

References to Index of Diseases and Injuries

The code 758.39 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • 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
  • Pneumatosis
  • Syndrome - see also Disease
    • antimongolism 758.39
    • autosomal - see also Abnormal, autosomes NEC
      • deletion 758.39
        • 5p 758.31
        • 22q11.2 758.32
    • chromosome 4 short arm deletion 758.39
    • deletion chromosomes 758.39
    • long arm 18 or 21 deletion 758.39

Crosswalk Information

The code 758.39 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
758.39 Right Arrow Q93.3 Deletion of short arm of chromosome 4
Q93.7 Deletions with other complex rearrangements
Q93.89 Other deletions from the autosomes
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
758.0 Down's syndrome
758.1 Patau's syndrome
758.2 Edwards' syndrome
758.31 Cri-du-chat syndrome
758.32 Velo-cardio-facial syndrome
758.33 Other microdeletions
758.4 Balanced autosomal translocation in normal individual
758.5 Other conditions due to autosomal anomalies
758.6 Gonadal dysgenesis
758.7 Klinefelter's syndrome
758.81 Other conditions due to sex chromosome anomalies
758.89 Other conditions due to chromosome anomalies
758.9 Conditions due to anomaly of unspecified chromosome


This page was last updated on: 10/1/2014