Q96.0
BillableKaryotype 45, X
Karyotype 45, X
Coding Notes
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)
Q96.1Karyotype 46, X iso (Xq)
Q96.2Karyotype 46, X w abnormal sex chromosome, except iso (Xq)
Q96.3Mosaicism, 45, X/46, XX or XY
Q96.4Mosaic, 45, X/other cell line(s) w abnormal sex chromosome
Q96.8Other variants of Turner's syndrome
Q96.9Turner's syndrome, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(43)
UMLS
- 45,XC0041408
- Gonadal DysgenesisC0041408
- Karyotype 45, XC0041408
- Pterygolymphangiectasia syndromeC0041408
- Syndrome, Ullrich-TurnerC0041408
- TS - Turner's syndromeC0041408
- Turner SyndromeC0041408
- Turner Syndrome (XO Syndrome)C0041408
- Turner syndromeC0041408
- Turner syndrome (disorder)C0041408
- Turner's SyndromeC0041408
- Turner's syndromeC0041408
- Turner's syndrome, unspecifiedC0041408
- Turners SyndromeC0041408
- Ullrich Turner SyndromeC0041408
- Ullrich-Turner SyndromeC0041408
- Ullrich-Turner syndromeC0041408
- XO SyndromeC0041408
- XO genotypeC0041408
- XO syndromeC0041408
- bonnevie-ullrich syndromeC0041408
- gonadal dysgenesisC0041408
- gonadal dysgenesis syndromeC0041408
- monosomy X syndromeC0041408
- turner's syndromeC0041408
- xo syndromeC0041408
Clinical Terms
- Ullrich-Turner Syndrome
- XO Syndrome
- Turners Syndrome
- Ullrich Turner Syndrome
- gonadal dysgenesis
- gonadal dysgenesis syndrome
- monosomy X syndrome
- bonnevie-ullrich syndrome
- TS - Turner's syndrome
- Turner syndrome (disorder)
- Turner Syndrome
- Pterygolymphangiectasia syndrome
- Syndrome, Ullrich-Turner
- Turner's syndrome, unspecified
- Turner Syndrome (XO Syndrome)
- 45,X
- XO genotype
Frequently Asked Questions
What is the ICD-10 code for karyotype 45, x?
The ICD-10-CM code for karyotype 45, x is Q96.0. The full clinical description is "Karyotype 45, X". Q96.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q96.0 mean?
ICD-10-CM code Q96.0 represents “Karyotype 45, X”. 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 Q96.0 a billable code?
Yes, Q96.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q96.0 in?
Q96.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q96.0?
Q96.0 has Excludes1 notes indicating codes that cannot be used together with it, including: Noonan syndrome (Q87.19).
What are the UMLS CUIs for Q96.0?
Q96.0 is linked to 1 UMLS Concept Unique Identifier: C0041408. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q96.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like karyotype 45, x 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 Q96.0?
Q96.0 maps to the ICD-11 code: LD50.00 (Karyotype 45, X).
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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.