Q93.52
BillablePhelan-McDermid syndrome
Phelan-McDermid syndrome
Status
Billable / Specific
Parent Code
Q93.5Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 22q13.3 deletion syndrome
Excludes 2
Conditions not included here, but the patient may have both
Use Additional Code
Additional codes that should follow this code
- code(s) to identify any associated conditions, such as:
- •autism spectrum disorderF84.0
- •degree of intellectual disabilitiesF70-F79
- •epilepsy and recurrent seizuresG40
- •lymphedemaI89.0
Related Codes(2)
Also Known As / Clinical Terms(27)
UMLS
- 22q13 Deletion SyndromeC1853490
- 22q13 deletion syndromeC1853490
- 22q13.3 Deletion SyndromeC1853490
- 22q13.3 deletion syndromeC1853490
- 22q13.3 deletion syndrome (disorder)C1853490
- CHROMOSOME 22q13.3 DELETION SYNDROMEC1853490
- Chromosome 22q13.3 Deletion SyndromeC1853490
- Deletion 22q13 SyndromeC1853490
- Deletion 22q13 syndromeC1853490
- Deletion 22q13.3 SyndromeC1853490
- Deletion 22q13.3 syndromeC1853490
- Monosomy 22q13C1853490
- PHELAN-MCDERMID SYNDROMEC1853490
- PHMDSC1853490
- Phelan-McDermid SyndromeC1853490
- Phelan-McDermid syndromeC1853490
- TELOMERIC 22q13 MONOSOMY SYNDROMEC1853490
- Telomeric 22q13 Monosomy SyndromeC1853490
Clinical Terms
- Monosomy 22q13
- 22q13 deletion syndrome
- PHMDS
- 22q13.3 deletion syndrome (disorder)
- Deletion 22q13 Syndrome
- TELOMERIC 22q13 MONOSOMY SYNDROME
- CHROMOSOME 22q13.3 DELETION SYNDROME
- 22q13.3 Deletion Syndrome
- Deletion 22q13.3 Syndrome
Frequently Asked Questions
What is the ICD-10 code for phelan-mcdermid syndrome?
The ICD-10-CM code for phelan-mcdermid syndrome is Q93.52. The full clinical description is "Phelan-McDermid syndrome". Q93.52 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q93.52 mean?
ICD-10-CM code Q93.52 represents “Phelan-McDermid syndrome”. 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 Q93.52 a billable code?
Yes, Q93.52 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q93.52 in?
Q93.52 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
Are additional codes required with Q93.52?
Yes, when using Q93.52, also report: code(s) to identify any associated conditions, such as:; autism spectrum disorder (F84.0); degree of intellectual disabilities (F70-F79); epilepsy and recurrent seizures (G40.-); lymphedema (I89.0).
What are the UMLS CUIs for Q93.52?
Q93.52 is linked to 1 UMLS Concept Unique Identifier: C1853490. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q93.52 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like phelan-mcdermid syndrome 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 Q93.52?
There is no direct ICD-11 mapping available for Q93.52 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.