ICD-10 Diagnosis Code Q93.88


Other microdeletions

Diagnosis Code Q93.88

ICD-10: Q93.88
Short Description: Other microdeletions
Long Description: Other microdeletions
This is the 2019 version of the ICD-10-CM diagnosis code Q93.88

Valid for Submission
The code Q93.88 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)
      • Monosomies and deletions from the autosomes, NEC (Q93)

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 Q93.88 is exempt from POA reporting.

Synonyms
  • 12q14 microdeletion syndrome
  • 12q15q21.1 microdeletion syndrome
  • 14q11.2 microdeletion syndrome
  • 14q12 microdeletion syndrome
  • 15q13.3 microdeletion
  • 15q14 microdeletion syndrome
  • 15q24 microdeletion
  • 16p partial trisomy syndrome
  • 16p11.2p12.2 microdeletion syndrome
  • 16p13.11 microduplication syndrome
  • 17q12 microdeletion syndrome
  • 17q23.1q23.2 microdeletion syndrome
  • 19p13.12 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
  • 20q13.33 microdeletion syndrome
  • 22q partial monosomy syndrome
  • 2p15p16.1 microdeletion syndrome
  • 2p21 microdeletion syndrome
  • 2q23.1 microdeletion syndrome
  • 2q24 microdeletion syndrome
  • 2q31.1 microdeletion syndrome
  • 2q32q33 microdeletion syndrome
  • 3q13 microdeletion syndrome
  • 3q29 microdeletion syndrome
  • 5q14.3 microdeletion syndrome
  • 6p22 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
  • Anomaly of chromosome pair 14
  • Anomaly of chromosome pair 14
  • Anomaly of chromosome pair 19
  • Anomaly of chromosome pair 3
  • Anomaly of chromosome pair 3
  • Anomaly of chromosome pair 5
  • 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 12
  • Deletion of part of chromosome 12
  • Deletion of part of chromosome 14
  • Deletion of part of chromosome 14
  • Deletion of part of chromosome 15
  • 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 19
  • Deletion of part of chromosome 2
  • Deletion of part of chromosome 2
  • Deletion of part of chromosome 2
  • Deletion of part of chromosome 2
  • Deletion of part of chromosome 2
  • Deletion of part of chromosome 2
  • 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 5
  • Deletion of part of chromosome 6
  • Deletion of part of chromosome 8
  • Deletion of part of chromosome 8
  • Deletion of part of chromosome 8
  • 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 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 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 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 6
  • Distal 16p11.2 microdeletion syndrome
  • Distal 22q11.2 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

Index of Diseases and Injuries
References found for the code Q93.88 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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