Q93.3
BillableDeletion of short arm of chromosome 4
Deletion of short arm of chromosome 4
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Wolff-Hirschorn syndrome
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(8)
Q93.0Whole chromosome monosomy,nonmosaic (meiotic nondisjunction)
Q93.1Whole chromosome monosomy, mosaic (mitotic nondisjunction)
Q93.2Chromosome replaced with ring, dicentric or isochromosome
Q93.4Deletion of short arm of chromosome 5
Q93.5Other deletions of part of a chromosome
Q93.7Deletions with other complex rearrangements
Q93.8Other deletions from the autosomes
Q93.9Deletion from autosomes, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(92)
SNOMED CT
- 4p minus syndrome17122004
- 4p partial monosomy syndrome17122004
- Chromosome 4 short arm deletion syndrome17122004
- Deletion of short arm of chromosome 417122004
- Midline fusion defect syndrome17122004
- Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)403757004
- Wolf Hirschhorn syndrome718226002
- Deletion of part of chromosome 4726371001
UMLS
- 4p Deletion SyndromeC1956097
- 4p Syndrome, ChromosomeC1956097
- 4p Syndromes, ChromosomeC1956097
- 4p deletion syndromeC1956097
- 4p minus syndromeC1956097
- 4p partial monosomy syndromeC1956097
- 4p partial monosomy syndrome (disorder)C1956097
- 4p syndromeC1956097
- 4p- SyndromeC1956097
- 4p- syndromeC1956097
- CHROMOSOME 4p16.3 DELETION SYNDROMEC1956097
- Chromosome 4 short arm deletion syndromeC1956097
- Chromosome 4p Deletion SyndromeC1956097
- Chromosome 4p MonosomyC1956097
- Chromosome 4p SyndromeC1956097
- Chromosome 4p SyndromesC1956097
- Chromosome 4p deletion syndromeC1956097
- Chromosome 4p monosomyC1956097
- Del(4p) SyndromeC1956097
- Del(4p) syndromeC1956097
- Deletion of short arm of chromosome 4C1956097
- Midline fusion defect syndromeC1956097
- Partial Monosomy 4pC1956097
- Partial monosomy 4pC1956097
- Syndrome, Chromosome 4pC1956097
- Syndrome, WolfC1956097
- Syndrome, Wolf-HirchhornC1956097
- Syndrome, Wolf-HirschhornC1956097
- Syndromes, Chromosome 4pC1956097
- WHSC1956097
- WOLF-HIRSCHHORN SYNDROMEC1956097
- Wolf Hirchhorn SyndromeC1956097
- Wolf Hirschhorn SyndromeC1956097
- Wolf Hirschhorn syndromeC1956097
- Wolf Hirschhorn syndrome (disorder)C1956097
- Wolf SyndromeC1956097
- Wolf-Hirchhorn SyndromeC1956097
- Wolf-Hirschhorn SyndromeC1956097
- Wolf-Hirschhorn syndromeC1956097
- Wolff-Hirschorn syndromeC1956097
- chromosome 4p deletion syndromeC1956097
- deletion 4p syndromeC1956097
- monosomy 4pC1956097
- syndrome wolfsC1956097
- syndromes wolfC1956097
- wolf syndromeC1956097
- wolf-hirschhorn syndromeC1956097
- wolff-hirschorn syndromeC1956097
Clinical Terms
- syndrome wolfs
- Syndrome, Wolf-Hirschhorn
- Chromosome 4p Deletion Syndrome
- Chromosome 4p monosomy
- Partial monosomy 4p
- Wolf Hirchhorn Syndrome
- Wolf-Hirschhorn syndrome
- Wolf-Hirchhorn Syndrome
- 4p syndrome
- monosomy 4p
- Wolf Hirschhorn syndrome (disorder)
- 4p Syndrome, Chromosome
- deletion 4p syndrome
- syndromes wolf
- 4p- syndrome
- Syndrome, Chromosome 4p
- 4p deletion syndrome
- 4p Syndromes, Chromosome
- wolff-hirschorn syndrome
- Wolf Hirschhorn syndrome
- Wolf Syndrome
- 4p partial monosomy syndrome (disorder)
- Del(4p) Syndrome
- Midline fusion defect syndrome
- Syndromes, Chromosome 4p
- Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
- 4p partial monosomy syndrome
- Chromosome 4p Syndrome
- 4p minus syndrome
- WHS
- Deletion of part of chromosome 4
- Syndrome, Wolf
- Syndrome, Wolf-Hirchhorn
- CHROMOSOME 4p16.3 DELETION SYNDROME
- Chromosome 4 short arm deletion syndrome
- Chromosome 4p Syndromes
Frequently Asked Questions
What is the ICD-10 code for deletion of short arm of chromosome 4?
The ICD-10-CM code for deletion of short arm of chromosome 4 is Q93.3. The full clinical description is "Deletion of short arm of chromosome 4". Q93.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q93.3 mean?
ICD-10-CM code Q93.3 represents “Deletion of short arm of chromosome 4”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q93.3 a billable code?
Yes, Q93.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q93.3 in?
Q93.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q93.3 map to?
Q93.3 maps to 4 SNOMED CT concepts: 17122004, 403757004, 726371001, 718226002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q93.3?
Q93.3 is linked to 1 UMLS Concept Unique Identifier: C1956097. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q93.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like deletion of short arm of chromosome 4 affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q93.3?
Q93.3 maps to the ICD-11 code: LD44.41 (Deletions of the short arm of chromosome 4).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.