Q96.2 – Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
ICD-10-CM 2027 diagnosis code · Chromosomal abnormalities, not elsewhere classified
ICD-10-CM code
Q96.2
- Code
Q96.2(claims format:Q962)- Description
- Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
- Short description
- Karyotype 46, X w abnormal sex chromosome, except iso (Xq)
- Billable
- Yes – valid for HIPAA-covered transactions
- Valid for
- Dates of service October 1, 2026 – September 30, 2027 (FY2027)
- Chapter
- 17. Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1)
- Block
- Q90-Q99 Chromosomal abnormalities, not elsewhere classified
- Parent codes
- Q96
Notes for Q96.2
Applicable to:
- Karyotype 46, X with abnormal sex chromosome, except isochromosome Xq
Notes inherited from parent codes
Instructional notes at a category or block level apply to every code below it.
Q96 – Turner's syndrome
Excludes1 (not coded here):
- Noonan syndrome (Q87.19)
Block Q90-Q99
Excludes2 (not included here):
- mitochondrial metabolic disorders (E88.4-)
Index terms for Q96.2
Entries in the ICD-10-CM alphabetic index that lead to this code:
Related codes in Q96
Frequently asked questions
What is ICD-10 code Q96.2?
Q96.2 is the ICD-10-CM code for karyotype 46, X with abnormal sex chromosome, except iso (Xq), in the block Q90-Q99 (Chromosomal abnormalities, not elsewhere classified).
Is Q96.2 a billable code?
Yes. Q96.2 is a billable/specific code that can be used to indicate a diagnosis for reimbursement purposes.
What category does Q96.2 belong to?
It belongs to category Q96 – Turner's syndrome.
Source: CDC/NCHS ICD-10-CM FY2027 code files, tabular list and index. Reference only – code assignment must follow the official ICD-10-CM guidelines and documentation in the medical record.