ICD-10-CM Code Q93.88

Other microdeletions

Version 2020 Billable Code POA Exempt

Valid for Submission

Q93.88 is a billable code used to specify a medical diagnosis of other microdeletions. The code is valid for the year 2020 for the submission of HIPAA-covered transactions. The ICD-10-CM code Q93.88 might also be used to specify conditions or terms like 10q partial monosomy syndrome, 10q22.3q23.3 microdeletion syndrome, 12p12.1 microdeletion syndrome, 12q14 microdeletion syndrome, 12q15q21.1 microdeletion syndrome, 13q partial monosomy syndrome, etc The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals.

ICD-10:Q93.88
Short Description:Other microdeletions
Long Description:Other microdeletions

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 Q93.88:

Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • Miller-Dieker syndrome
  • Smith-Magenis syndrome

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code Q93.88 are found in the index:


Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • 10q partial monosomy syndrome
  • 10q22.3q23.3 microdeletion syndrome
  • 12p12.1 microdeletion syndrome
  • 12q14 microdeletion syndrome
  • 12q15q21.1 microdeletion syndrome
  • 13q partial monosomy syndrome
  • 13q12.3 microdeletion syndrome
  • 14q11.2 microdeletion syndrome
  • 14q12 microdeletion syndrome
  • 14q22q23 microdeletion syndrome
  • 14q24.1q24.3 microdeletion syndrome
  • 15q11.2 microdeletion syndrome
  • 15q13.3 microdeletion
  • 15q14 microdeletion syndrome
  • 15q24 microdeletion
  • 16p partial trisomy syndrome
  • 16p11.2p12.2 microdeletion syndrome
  • 16p12.2 microdeletion syndrome
  • 16p13.11 microduplication syndrome
  • 16q partial monosomy syndrome
  • 16q24.1 microdeletion syndrome
  • 17q12 microdeletion syndrome
  • 17q23.1q23.2 microdeletion syndrome
  • 19p13.12 microdeletion syndrome
  • 19p13.13 microdeletion syndrome
  • 1p partial monosomy syndrome
  • 1p31p32 microdeletion syndrome
  • 1q partial monosomy syndrome
  • 1q partial monosomy syndrome
  • 1q partial monosomy syndrome
  • 1q21.1 microdeletion
  • 1q41q42 microdeletion syndrome
  • 1q44 microdeletion syndrome
  • 20p12.3 microdeletion syndrome
  • 20p13 microdeletion syndrome
  • 20q13.33 microdeletion syndrome
  • 22q partial monosomy syndrome
  • 2p13.2 microdeletion syndrome
  • 2p15p16.1 microdeletion syndrome
  • 2p21 microdeletion syndrome
  • 2p21 microdeletion syndrome without cystinuria
  • 2q23.1 microdeletion syndrome
  • 2q24 microdeletion syndrome
  • 2q31.1 microdeletion syndrome
  • 2q32q33 microdeletion syndrome
  • 2q33.1 microdeletion syndrome
  • 3q13 microdeletion syndrome
  • 3q26q27 microdeletion syndrome
  • 3q27.3 microdeletion syndrome
  • 3q29 microdeletion syndrome
  • 5q14.3 microdeletion syndrome
  • 5q31.3 microdeletion syndrome
  • 6p22 microdeletion syndrome
  • 7q partial monosomy syndrome
  • 7q partial monosomy syndrome
  • 7q31 microdeletion syndrome
  • 8p partial monosomy syndrome
  • 8p23.1 microdeletion syndrome
  • 8q partial monosomy syndrome
  • 8q partial monosomy syndrome
  • 8q13 microdeletion syndrome
  • 8q22.1 microdeletion syndrome
  • 9p13 microdeletion syndrome
  • 9q partial monosomy syndrome
  • 9q31.1q31.3 microdeletion syndrome
  • Chromosome 16p11.2 deletion syndrome
  • Chromosome microdeletion
  • Chromosome Xp11.3 microdeletion syndrome
  • Chromosome Xp22.3 microdeletion syndrome
  • Deletion of part of chromosome 1
  • Deletion of part of chromosome 1
  • Deletion of part of chromosome 1
  • Deletion of part of chromosome 1
  • Deletion of part of chromosome 10
  • Deletion of part of chromosome 12
  • Deletion of part of chromosome 12
  • Deletion of part of chromosome 12
  • Deletion of part of chromosome 13
  • Deletion of part of chromosome 14
  • Deletion of part of chromosome 14
  • Deletion of part of chromosome 14
  • Deletion of part of chromosome 14
  • Deletion of part of chromosome 15
  • Deletion of part of chromosome 15
  • Deletion of part of chromosome 16
  • Deletion of part of chromosome 16
  • Deletion of part of chromosome 16
  • Deletion of part of chromosome 16
  • Deletion of part of chromosome 17
  • Deletion of part of chromosome 17
  • Deletion of part of chromosome 17
  • Deletion of part of chromosome 17
  • Deletion of part of chromosome 19
  • Deletion of part of chromosome 19
  • Deletion of part of chromosome 20
  • Deletion of part of chromosome 20
  • Deletion of part of chromosome 20
  • Deletion of part of chromosome 20
  • Deletion of part of chromosome 22
  • Deletion of part of chromosome 3
  • Deletion of part of chromosome 3
  • Deletion of part of chromosome 3
  • Deletion of part of chromosome 3
  • Deletion of part of chromosome 5
  • Deletion of part of chromosome 5
  • Deletion of part of chromosome 6
  • Deletion of part of chromosome 7
  • Deletion of part of chromosome 7
  • Deletion of part of chromosome 8
  • Deletion of part of chromosome 8
  • Deletion of part of chromosome 8
  • Deletion of part of chromosome 9
  • Deletion of part of chromosome 9
  • Deletion of part of long arm of chromosome 12
  • Deletion of part of long arm of chromosome 12
  • Deletion of part of long arm of chromosome 17
  • Deletion of part of long arm of chromosome 17
  • Deletion of part of long arm of chromosome 2
  • Deletion of part of long arm of chromosome 2
  • Deletion of part of long arm of chromosome 2
  • Deletion of part of long arm of chromosome 2
  • Deletion of part of long arm of chromosome 2
  • Deletion of part of long arm of chromosome 20
  • Deletion of part of long arm of chromosome 20
  • Deletion of part of long arm of chromosome 3
  • Deletion of part of long arm of chromosome 3
  • Deletion of part of long arm of chromosome 3
  • Deletion of part of long arm of chromosome 3
  • Deletion of part of long arm of chromosome 5
  • Deletion of part of long arm of chromosome 5
  • Deletion of part of short arm of chromosome 16
  • Deletion of part of short arm of chromosome 16
  • Deletion of part of short arm of chromosome 16
  • Deletion of part of short arm of chromosome 17
  • Deletion of part of short arm of chromosome 17
  • Deletion of part of short arm of chromosome 2
  • Deletion of part of short arm of chromosome 2
  • Deletion of part of short arm of chromosome 2
  • Deletion of part of short arm of chromosome 2
  • Deletion of part of short arm of chromosome 20
  • Deletion of part of short arm of chromosome 20
  • Deletion of part of short arm of chromosome 6
  • Deletion of short arm of chromosome 19
  • Deletion of short arm of chromosome 19
  • Distal 16p11.2 microdeletion syndrome
  • Distal 17p13.1 microdeletion syndrome
  • Distal 17p13.3 microdeletion syndrome
  • Distal 22q11.2 microdeletion syndrome
  • Distal 7q11.23 microdeletion syndrome
  • Miller Dieker syndrome
  • Osteopoikilosis
  • Partial trisomy of chromosome 16
  • Paternal 20q13.2q13.3 microdeletion syndrome
  • Proximal 16p11.2 microdeletion syndrome
  • Smith-Magenis syndrome
  • Type 1 lissencephaly

Present on Admission (POA)

Q93.88 is exempt from POA reporting - 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. Review other POA exempt codes here .

CMS POA Indicator Options and Definitions
POA Indicator CodePOA Reason for CodeCMS will pay the CC/MCC DRG?
YDiagnosis was present at time of inpatient admission.YES
NDiagnosis was not present at time of inpatient admission.NO
UDocumentation insufficient to determine if the condition was present at the time of inpatient admission.NO
WClinically undetermined - unable to clinically determine whether the condition was present at the time of inpatient admission.YES
1Unreported/Not used - Exempt from POA reporting. NO

Convert Q93.88 to ICD-9

Code Classification

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Chromosomal abnormalities, not elsewhere classified (Q90-Q99)
      • Monosomies and deletions from the autosomes, NEC (Q93)

Code History

  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016
    (First year ICD-10-CM implemented into the HIPAA code set)
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020

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


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