Q96.9
BillableTurner's syndrome, unspecified
Turner's syndrome, unspecified
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)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(74)
SNOMED CT
- Genetic mosaic17523003
- Bonnevie-Ullrich syndrome38804009
- Gonadal dysgenesis syndrome38804009
- Pterygolymphangiectasia syndrome38804009
- TS - Turner's syndrome38804009
- Turner syndrome38804009
- Turner's syndrome38804009
- Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance93466004
- Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance93466004
- Perrault syndrome93466004
- Gonadal dysgenesis205681004
- Ovarian dysgenesis205683001
- Congenital anomaly of endocrine ovary370966000
- 45, X syndrome710008008
- 45XO - Turner's syndrome710008008
- Karyotype 45, X710008008
- Monosomy X710008008
- XO - Turner's syndrome710008008
- XO syndrome710008008
- Mosaic Turner syndrome710010005
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
- Congenital anomaly of endocrine ovary
- Ullrich-Turner Syndrome
- Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
- XO Syndrome
- Perrault syndrome
- Turners Syndrome
- Ullrich Turner Syndrome
- gonadal dysgenesis
- Gonadal dysgenesis syndrome
- 45, X syndrome
- Bonnevie-Ullrich syndrome
- monosomy X syndrome
- TS - Turner's syndrome
- Turner syndrome (disorder)
- Turner Syndrome
- Pterygolymphangiectasia syndrome
- Syndrome, Ullrich-Turner
- Turner Syndrome (XO Syndrome)
- 45XO - Turner's syndrome
- 45,X
- Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance
- Mosaic Turner syndrome
- Ovarian dysgenesis
- Monosomy X
- Genetic mosaic
- XO genotype
- XO - Turner's syndrome
- Karyotype 45, X
Frequently Asked Questions
What is the ICD-10 code for turner's syndrome, unspecified?
The ICD-10-CM code for turner's syndrome, unspecified is Q96.9. The full clinical description is "Turner's syndrome, unspecified". Q96.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q96.9 mean?
ICD-10-CM code Q96.9 represents “Turner's syndrome, unspecified”. 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 Q96.9 a billable code?
Yes, Q96.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q96.9 in?
Q96.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q96.9?
Q96.9 has Excludes1 notes indicating codes that cannot be used together with it, including: Noonan syndrome (Q87.19).
What SNOMED CT codes does Q96.9 map to?
Q96.9 maps to 8 SNOMED CT concepts: 710008008, 38804009, 370966000, 17523003, 205681004, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q96.9?
Q96.9 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 Q96.9 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like turner's syndrome, unspecified 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 Q96.9?
Q96.9 maps to the ICD-11 code: LD50.04 (Mosaicism, 45, X or other cell line with abnormal sex chromosome).
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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.