DxCodebookFY2027 · Oct 1, 2026 – Sep 30, 2027

Category · FY2027

Q96 Turner's syndrome

  • Header · not billable

Q96 is not billable. The category heads 7 billable codes in FY2027: the 7 codes directly below it.

Index → code

  • XO syndrome → Q96.9
  • Turner-Ullrich syndrome → Q96.9
  • Morgagni-Turner (-Albright) syndrome → Q96.9

Where it sits

  1. Chapter 17 Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1)
  2. Q90-Q99 Chromosomal abnormalities, not elsewhere classified (Q90-Q99)
  3. Q96 Turner's syndrome
Billable codes
7
Subdivisions
7
CC / MCC codes
0 / 0
HCC V28 codes
0
New FY2027
0
Index entries
15

Codes in Q96

  1. Q96.0
    Karyotype 45, X
    BillableExempt
  2. Q96.1
    Karyotype 46, X iso (Xq)
    BillableExempt
    Inclusion terms 1

    Inclusion terms

    • Karyotype 46, isochromosome Xq
  3. Q96.2
    Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
    BillableExempt
    Inclusion terms 1

    Inclusion terms

    • Karyotype 46, X with abnormal sex chromosome, except isochromosome Xq
  4. Q96.3
    Mosaicism, 45, X/46, XX or XY
    BillableExempt
  5. Q96.4
    Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
    BillableExempt
  6. Q96.8
    Other variants of Turner's syndrome
    BillableExempt
  7. Q96.9
    Turner's syndrome, unspecified
    BillableExempt

Sources of each column.

Instructions

At Q96

Excludes1

  • Noonan syndrome (Q87.19) Q87.19

Notes that also apply

Block Q90-Q99 instructions (Excludes2 1): printed on the block page.

Chapter 17 instructions (Notes 1, Excludes2 1): printed on the chapter 17 page.

Index entries

  • Morgagni-Turner (-Albright) syndrome → Q96.9
  • Turner-Ullrich syndrome → Q96.9
  • XO syndrome → Q96.9
  • Karyotype45,X → Q96.0
  • Karyotypewith abnormality except iso (Xq) → Q96.2
  • Mosaicism, mosaic (autosomal) (chromosomal)45,X/46,XX → Q96.3
  • Mosaicism, mosaic (autosomal) (chromosomal)XY → Q96.3
  • Mosaicism, mosaic (autosomal) (chromosomal)45,X/other cell lines NEC with abnormal sex chromosome → Q96.4
  • Dysgenesisgonadal (due to chromosomal anomaly) → Q96.9
  • MonosomyX → Q96.9
  • Turner'ssyndrome → Q96.9
  • Karyotype46,Xiso (Xq) → Q96.1
  • Turner'ssyndromespecified NEC → Q96.8
  • Anomaly, anomalous (congenital) (unspecified type)chromosomes, chromosomalsexTurner's → Q96.9
  • Deficiency, deficientshort stature homeobox gene (SHOX)withTurner's syndrome → Q96.9

NCHS Alphabetic Index. Index first, then the Tabular List.

Hierarchy