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ICD-10-CM Codes
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Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities
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Q90-Q99
Chromosomal abnormalities, not elsewhere classified
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Q93-
Monosomies and deletions from the autosomes, not elsewhere classified
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2021 ICD-10-CM Diagnosis Code Q93.81
2021 ICD-10-CM Diagnosis Code Q93.81
Velo-cardio-facial syndrome
2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
- Q93.81 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2021 edition of ICD-10-CM Q93.81 became effective on October 1, 2020.
- This is the American ICD-10-CM version of Q93.81 - other international versions of ICD-10 Q93.81 may differ.
The following code(s) above
Q93.81 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q93.81:
- 22q deletion
- Digeorges syndrome
- Shprintzen syndrome
- Velo cardio facial syndrome
Clinical Information
- Caused by microdeletion on chromosome 22q11.2; associated with multiple congenital anomalies, learning disabilities, behavioral phenotypes including adhd and anxiety, with schizophrenic risk in adulthood.
- Typical facies with a prominent nose and retruded mandible, cleft palate, cardiovascular defects, learning disability, retarded mental development, and short stature. Elements of this syndrome are frequently present in the robin syndrome.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q93.81 is considered exempt from POA reporting.
ICD-10-CM Q93.81 is grouped within Diagnostic Related Group(s) (MS-DRG v38.0):
- 884 Organic disturbances and intellectual disability
Convert Q93.81 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
ICD-10-CM Codes Adjacent To Q93.81
Q93.0 Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q93.2 Chromosome replaced with ring, dicentric or isochromosome
Q93.3 Deletion of short arm of chromosome 4
Q93.4 Deletion of short arm of chromosome 5
Q93.5 Other deletions of part of a chromosome
Q93.59 Other deletions of part of a chromosome
Q93.7 Deletions with other complex rearrangements
Q93.8 Other deletions from the autosomes
Q93.81
Velo-cardio-facial syndrome
Q93.89 Other deletions from the autosomes
Q93.9 Deletion from autosomes, unspecified
Q95 Balanced rearrangements and structural markers, not elsewhere classified
Q95.0 Balanced translocation and insertion in normal individual
Q95.1 Chromosome inversion in normal individual
Q95.2 Balanced autosomal rearrangement in abnormal individual
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual
Q95.5 Individual with autosomal fragile site
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
