Q96.2
BillableKaryotype 46, X w abnormal sex chromosome, except iso (Xq)
Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Karyotype 46, X with abnormal sex chromosome, except isochromosome Xq
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(6)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(20)
SNOMED CT
UMLS
- Karyotype 46, X w abnormal sex chromosome, except iso (Xq)C0432464
- Karyotype 46, X with abnormal sex chromosome except iso (Xq)C0432464
- Karyotype 46, X with abnormal sex chromosome except iso (Xq) (disorder)C0432464
- Karyotype 46, X with abnormal sex chromosome, except iso (Xq)C0432464
- Karyotype 46, X with abnormal sex chromosome, except isochromosome XqC2910376
Clinical Terms
- Gonadal dysgenesis syndrome
- Karyotype 46, X with abnormal sex chromosome except iso (Xq)
- Bonnevie-Ullrich syndrome
- Karyotype 46, X with abnormal sex chromosome except iso (Xq) (disorder)
- TS - Turner's syndrome
- Pterygolymphangiectasia syndrome
- Turner syndrome
- Karyotype 46, X with abnormal sex chromosome, except isochromosome Xq
Frequently Asked Questions
What is the ICD-10 code for karyotype 46, x w abnormal sex chromosome, except iso (xq)?
The ICD-10-CM code for karyotype 46, x w abnormal sex chromosome, except iso (xq) is Q96.2. The full clinical description is "Karyotype 46, X with abnormal sex chromosome, except iso (Xq)". Q96.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q96.2 mean?
ICD-10-CM code Q96.2 represents “Karyotype 46, X with abnormal sex chromosome, except iso (Xq)”. 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 Q96.2 a billable code?
Yes, Q96.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q96.2 in?
Q96.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q96.2?
Q96.2 has Excludes1 notes indicating codes that cannot be used together with it, including: Noonan syndrome (Q87.19).
What SNOMED CT codes does Q96.2 map to?
Q96.2 maps to 2 SNOMED CT concepts: 38804009, 205687000. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q96.2?
Q96.2 is linked to 2 UMLS Concept Unique Identifiers: C0432464, C2910376. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q96.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like karyotype 46, x w abnormal sex chromosome, except iso (xq) 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 Q96.2?
Q96.2 maps to the ICD-11 code: LD50.02 (Karyotype 46, X with abnormal sex chromosome, except iso Xq).
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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.