Not Valid for Submission
Q92 is a "header" nonspecific and non-billable diagnosis code code, consider using a code with a higher level of specificity for a diagnosis of other trisomies and partial trisomies of the autosomes, not elsewhere classified. The code is NOT valid for the year 2021 for the submission of HIPAA-covered transactions. Category or Header define the heading of a category of codes that may be further subdivided by the use of 4th, 5th, 6th or 7th characters.
Specific Coding for Oth trisomies and partial trisomies of the autosomes, NEC
Header codes like Q92 require more digits to indicate the appropriate level of specificity. Consider using any of the following ICD-10 codes with a higher level of specificity when coding for oth trisomies and partial trisomies of the autosomes, nec:
- Q92.0 - Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
- Q92.1 - Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
- Q92.2 - Partial trisomy
- Q92.5 - Duplications with other complex rearrangements
- Q92.6 - Marker chromosomes
- Q92.61 - Marker chromosomes in normal individual
- Q92.62 - Marker chromosomes in abnormal individual
- Q92.7 - Triploidy and polyploidy
- Q92.8 - Other specified trisomies and partial trisomies of autosomes
- Q92.9 - Trisomy and partial trisomy of autosomes, unspecified
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code Q92:
This note appears immediately under a three character code title to further define, or give examples of, the content of the category.
- unbalanced translocations and insertions
Type 1 ExcludesType 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
Information for Patients
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 (Medical Encyclopedia)