758.5 AUTOSOMAL ANOMALIES NEC


Code Information

Diagnosis Code: 758.5

Short Description: Autosomal anomalies NEC

Long Description: Other conditions due to autosomal anomalies

Code Classification:

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

Code Version: 2015 ICD-9-CM


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
  • 22q11.2 duplication
  • 2q partial trisomy syndrome
  • 3p partial monosomy 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 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
  • Pitt-Hopkins syndrome
  • Pyle metaphyseal dysplasia
  • SOX2 anophthalmia syndrome
  • Supernumerary der
  • 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

References to Index of Diseases and Injuries

The code 758.5 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Abnormal, abnormality, abnormalities - see also Anomaly
    • autosomes NEC 758.5
      • 13 758.1
      • 18 758.2
      • 21 or 22 758.0
      • D1�758.1
      • E3�758.2
      • G 758.0
    • chromosomal NEC 758.89
      • autosomes (see also Abnormal, autosomes NEC) 758.5
  • Accessory (congenital)
    • autosome(s) NEC 758.5
      • 21 or 22 758.0
    • chromosome(s) NEC 758.5
      • 13-15 758.1
      • 16-18 758.2
      • 21 or 22 758.0
      • autosome(s) NEC 758.5
      • D1�758.1
      • E3�758.2
      • G 758.0
      • sex 758.81
  • Additional - see also Accessory
    • chromosome(s) 758.5
      • 13-15 758.1
      • 16-18 758.2
      • 21 758.0
      • autosome(s) NEC 758.5
      • sex 758.81
  • Aneuploidy NEC 758.5
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
    • autosomes, autosomal NEC 758.5
    • chromosomes, chromosomal 758.9
      • autosomes NEC (see also Abnormal, autosomes) 758.5
        • deletion 758.39
  • Mosaicism, mosaic (chromosomal) 758.9
    • autosomal 758.5
  • Paratyphoid (fever) - see Fever, paratyphoid
  • Syndrome - see also Disease
    • due to abnormality
      • autosomal NEC (see also Abnormal, autosomes NEC) 758.5
        • 13 758.1
        • 18 758.2
        • 21 or 22 758.0
        • D1�758.1
        • E3�758.2
        • G 758.0
    • trisomy NEC 758.5
      • 13 or D1�758.1
      • 16-18 or E 758.2
      • 18 or E3�758.2
      • 20 758.5
      • 21 or G (mongolism) 758.0
      • 22 or G (mongolism) 758.0
      • G 758.0
  • Translocation
    • autosomes NEC 758.5
      • 13-15 758.1
      • 16-18 758.2
      • 21 or 22 758.0
      • balanced in normal individual 758.4
      • D1�758.1
      • E3�758.2
      • G 758.0
  • Trisomy (syndrome) NEC 758.5
    • 13 (partial) 758.1
    • 16-18 758.2
    • 18 (partial) 758.2
    • 21 (partial) 758.0
    • 22 758.0
    • autosomes NEC 758.5
    • D1�758.1
    • E3�758.2
    • G (group) 758.0
    • group D1�758.1
    • group E 758.2
    • group G 758.0

Crosswalk Information

The code 758.5 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
758.5 Right Arrow Q92.8 Other specified trisomies and partial trisomies of 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
758.39 Other autosomal deletions
758.4 Balanced autosomal translocation in normal individual
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