ICD-10 Diagnosis Code Q92.8

Other specified trisomies and partial trisomies of autosomes

Diagnosis Code Q92.8

ICD-10: Q92.8
Short Description: Other specified trisomies and partial trisomies of autosomes
Long Description: Other specified trisomies and partial trisomies of autosomes
This is the 2018 version of the ICD-10-CM diagnosis code Q92.8

Valid for Submission
The code Q92.8 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Chromosomal abnormalities, not elsewhere classified (Q90-Q99)
      • Oth trisomies and partial trisomies of the autosomes, NEC (Q92)

Information for Medical Professionals

Convert to ICD-9 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.

Present on Admission (POA) Additional informationCallout TooltipPresent on Admission
The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement.

The code Q92.8 is exempt from POA reporting.

Synonyms
  • 10p partial trisomy syndrome
  • 12p partial trisomy syndrome
  • 14q partial distal trisomy syndrome
  • 14q partial proximal trisomy syndrome
  • 14q partial trisomy syndrome
  • 14q partial trisomy syndrome
  • 15q partial trisomy syndrome
  • 16p partial trisomy syndrome
  • 16q partial trisomy syndrome
  • 18p partial trisomy syndrome
  • 19q partial trisomy syndrome
  • 1q partial trisomy syndrome
  • 20p partial trisomy syndrome
  • 20q partial trisomy syndrome
  • 22q partial trisomy syndrome
  • 22q11.2 duplication
  • 3q partial trisomy syndrome
  • 4p partial trisomy syndrome
  • 4q partial trisomy syndrome
  • 5p partial trisomy syndrome
  • 6q partial trisomy syndrome
  • 8q partial trisomy syndrome
  • Anomaly of chromosome pair 1
  • Anomaly of chromosome pair 10
  • Anomaly of chromosome pair 10
  • Anomaly of chromosome pair 12
  • Anomaly of chromosome pair 14
  • Anomaly of chromosome pair 14
  • Anomaly of chromosome pair 14
  • Anomaly of chromosome pair 15
  • Anomaly of chromosome pair 16
  • Anomaly of chromosome pair 16
  • Anomaly of chromosome pair 16
  • Anomaly of chromosome pair 19
  • Anomaly of chromosome pair 20
  • Anomaly of chromosome pair 20
  • Anomaly of chromosome pair 20
  • Anomaly of chromosome pair 22
  • Anomaly of chromosome pair 22
  • Anomaly of chromosome pair 22
  • Anomaly of chromosome pair 22
  • Anomaly of chromosome pair 3
  • Anomaly of chromosome pair 4
  • Anomaly of chromosome pair 4
  • Anomaly of chromosome pair 5
  • Anomaly of chromosome pair 6
  • Anomaly of chromosome pair 8
  • Anomaly of chromosome pair 8
  • Anomaly of chromosome pair 9
  • Cat eye syndrome
  • Complete trisomy 10 syndrome
  • Complete trisomy 14 syndrome
  • Complete trisomy 16 syndrome
  • Complete trisomy 20 syndrome
  • Complete trisomy 22 syndrome
  • Complete trisomy 8 syndrome
  • Complete trisomy 9 syndrome
  • Duplication of chromosome
  • Duplication of chromosome
  • Duplication seen only at prometaphase
  • Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
  • Pseudotrisomy 18
  • Trisomy 10
  • Trisomy 11
  • Trisomy 12
  • Trisomy 22
  • Trisomy 6
  • Trisomy 7
  • Trisomy 8
  • Trisomy 9

Index of Diseases and Injuries
References found for the code Q92.8 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 (Medical Encyclopedia)


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