ICD-9 Diagnosis Code 758.39

Autosomal deletions NEC

Diagnosis Code 758.39

ICD-9: 758.39
Short Description: Autosomal deletions NEC
Long Description: Other autosomal deletions
This is the 2014 version of the ICD-9-CM diagnosis code 758.39

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.

  • 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

Index of Diseases and Injuries
References found for the code 758.39 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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