ICD-9 Diagnosis Code 758.5

Autosomal anomalies NEC

Diagnosis Code 758.5

ICD-9: 758.5
Short Description: Autosomal anomalies NEC
Long Description: Other conditions due to autosomal anomalies
This is the 2014 version of the ICD-9-CM diagnosis code 758.5

Code Classification
  • Congenital anomalies (740–759)
    • 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.

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

Index of Diseases and Injuries
References found for the code 758.5 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


[Read More]
Previous Code
Previous Code 758.4
Next Code
758.6 Next Code