ICD-9 Diagnosis Code 758.89

Oth con d/t chrm anm NEC

Diagnosis Code 758.89

ICD-9: 758.89
Short Description: Oth con d/t chrm anm NEC
Long Description: Other conditions due to chromosome anomalies
This is the 2014 version of the ICD-9-CM diagnosis code 758.89

Code Classification
  • Congenital anomalies
    • Congenital anomalies (740-759)
      • 758 Chromosomal anomalies

Information for Medical Professionals

Convert to ICD-10 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • 14q partial distal trisomy syndrome
  • 14q partial proximal trisomy syndrome
  • 14q partial trisomy syndrome
  • 16p partial trisomy syndrome
  • 16q partial monosomy syndrome
  • 2p partial trisomy syndrome
  • Anomaly of chromosome pair 1
  • Anomaly of chromosome pair 10
  • Anomaly of chromosome pair 11
  • Anomaly of chromosome pair 12
  • Anomaly of chromosome pair 14
  • Anomaly of chromosome pair 15
  • Anomaly of chromosome pair 16
  • Anomaly of chromosome pair 17
  • Anomaly of chromosome pair 19
  • Anomaly of chromosome pair 2
  • Anomaly of chromosome pair 20
  • Anomaly of chromosome pair 21
  • Anomaly of chromosome pair 3
  • Anomaly of chromosome pair 4
  • Anomaly of chromosome pair 5
  • Anomaly of chromosome pair 6
  • Anomaly of chromosome pair 7
  • Anomaly of chromosome pair 8
  • Anomaly of chromosome pair 9
  • Balanced autosomal rearrangement in abnormal individual
  • Balanced autosomal translocation
  • Balanced rearrangement and structural marker
  • Balanced sex/autosomal rearrangement in abnormal individual
  • Balanced translocation and insertion in normal individual
  • Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
  • Chromosomal alterations of group A
  • Chromosomal alterations of group B
  • Chromosomal alterations of group C and X
  • Chromosomal alterations of group D
  • Chromosomal alterations of group E
  • Chromosomal alterations of group F
  • Chromosomal alterations of group G and Y
  • Chromosomal disorder
  • Complete trisomy 14 syndrome
  • Complete trisomy 16 syndrome
  • Duplication of chromosome
  • Duplication with other complex rearrangement
  • Extra unidentified structurally abnormal chromosome
  • Familial extra unidentified structurally abnormal chromosome
  • Group chromosomal alteration
  • Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
  • Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation
  • Male with sex chromosome mosaicism
  • Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
  • Mitochondrial mutation
  • Monosomy 21, mosaicism
  • Mosaic variegated aneuploidy syndrome
  • Opitz-Frias syndrome
  • Pallister-Killian syndrome
  • Partial tetrasomy 9 syndrome
  • Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
  • Ring chromosome 1 syndrome
  • Ring chromosome 10 syndrome
  • Ring chromosome 11 syndrome
  • Ring chromosome 14 syndrome
  • Ring chromosome 18 syndrome
  • Ring chromosome 20 syndrome
  • Ring chromosome 21 syndrome
  • Ring chromosome 4 syndrome
  • Ring chromosome 9 syndrome
  • Schöpf-Schulz-Passarge syndrome
  • Snyder-Robinson x-linked mental retardation syndrome
  • Spondylocarpotarsal synostosis syndrome
  • Spondyloepimetaphyseal dysplasia, Strudwick type
  • Spondyloperipheral dysplasia
  • Tetrasomy 18p
  • Triploidy syndrome
  • Triploidy, diploidy, mixoploidy syndrome
  • Unbalanced translocation of chromosome
  • Whole chromosome monosomy - meiotic nondisjunction
  • Whole chromosome trisomy syndrome
  • Whole chromosome trisomy, meiotic nondisjunction
  • Whole chromosome trisomy, mosaicism
  • X-linked mental retardation, syndromic 13

Index of Diseases and Injuries
References found for the code 758.89 in the Index of Diseases and Injuries:

Information for Patients

Genetic Disorders

Genes are the building blocks of heredity. They are passed from parent to child. They hold DNA, the instructions for making proteins. Proteins do most of the work in cells. They move molecules from one place to another, build structures, break down toxins, and do many other maintenance jobs.

Sometimes there is a mutation, a change in a gene or genes. The mutation changes the gene's instructions for making a protein, so the protein does not work properly or is missing entirely. This can cause a medical condition called a genetic disorder.

You can inherit a gene mutation from one or both parents. A mutation can also happen during your lifetime.

There are three types of genetic disorders:

  • Single-gene disorders, where a mutation affects one gene. Sickle cell anemia is an example.
  • Chromosomal disorders, where chromosomes (or parts of chromosomes) are missing or changed. Chromosomes are the structures that hold our genes. Down syndrome is a chromosomal disorder.
  • Complex disorders, where there are mutations in two or more genes. Often your lifestyle and environment also play a role. Colon cancer is an example.

Genetic tests on blood and other tissue can identify genetic disorders.

NIH: National Library of Medicine

  • Genetics

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