Q98.0

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Q98.0

Billable

Klinefelter syndrome karyotype 47, XXY

Q98.0 is the ICD-10-CM code for Klinefelter syndrome karyotype 47, XXY. It is a billable, specific code valid for reimbursement.

Status
Billable
Chapter
Q00-Q99
Parent
Q98
Edition
FY2026

Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities

What this means — in plain language

MedlinePlus · NIH

What is Klinefelter syndrome (KS)? Klinefelter syndrome (KS) is a genetic condition that happens when a male is born with an extra copy of the X chromosome. KS can affect different stages of physical, language, and social development. It also usually causes infertility . What causes Klinefelter syndrome (KS)? KS is not inherited. It's caused by a random error that happens when a sperm or egg is formed. This error…

Read more about Klinefelter Syndrome at MedlinePlus ↗

Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.

No additional coding notes for this code.

Conditions mapped to this code

MedlinePlus · NIH

Plain-language health-topic references grounded in MedlinePlus (NIH/NLM).

Frequently asked questions

What is ICD-10 code Q98.0?
Q98.0 is the ICD-10-CM code for "Klinefelter syndrome karyotype 47, XXY". It falls under Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities.
Is Q98.0 a billable code?
Yes — Q98.0 is a billable, specific ICD-10-CM code valid for reimbursement.

Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.

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