Q98.0
BillableKlinefelter syndrome karyotype 47, XXY
Klinefelter syndrome karyotype 47, XXY
Status
Billable / Specific
Parent Code
Q98Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Klinefelter syndrome22053006
- Klinefelter's syndrome22053006
- Sex phenotype-karyotype dissociation syndrome36114005
- Male with 46, XX karyotype74398009
- XX males74398009
- Klinefelter syndrome, male with 46,XX karyotype205698004
- Klinefelter's syndrome, male with 46,XX karyotype205698004
- Sex chromosome mosaicism205706002
- Mosaic XY/XXY205709009
- Klinefelter syndrome, XXY405769009
- Klinefelter's syndrome karyotype 47 XXY405769009
- Klinefelter's syndrome, XXY405769009
- XXY Klinefelter's syndrome405769009
- XXY syndrome405769009
UMLS
- 47,XXY syndromeC0022735
- Hypogonadism, primaryC0022735
- Hypogonadotropic HypogonadismC0022735
- Klinefelter SyndromeC0022735
- Klinefelter SyndromesC0022735
- Klinefelter syndromeC0022735
- Klinefelter syndrome (KS)C0022735
- Klinefelter syndrome (disorder)C0022735
- Klinefelter syndrome karyotype 47, XXYC0022735
- Klinefelter syndrome, XXYC0022735
- Klinefelter syndrome, unspecifiedC0022735
- Klinefelter's SyndromeC0022735
- Klinefelter's syndromeC0022735
- Klinefelter's syndrome karyotype 47 XXYC0022735
- Klinefelter's syndrome, XXYC0022735
- Klinefelter's syndrome, XXY (disorder)C0022735
- Klinefelters SyndromeC0022735
- Syndrome, KlinefelterC0022735
- Syndrome, Klinefelter'sC0022735
- Syndrome, XXYC0022735
- Syndromes, KlinefelterC0022735
- Syndromes, XXYC0022735
- XXY Klinefelter's syndromeC0022735
- XXY SyndromeC0022735
- XXY Syndrome (Klinefelter Syndrome)C0022735
- XXY SyndromesC0022735
- XXY maleC0022735
- XXY syndromeC0022735
- XXY trisomyC0022735
- chromosome xxy syndromeC0022735
- hypogonadotropic hypogonadismC0022735
- klinefelter 's syndromeC0022735
- klinefelter diseaseC0022735
- klinefelter syndromeC0022735
- klinefelter's syndromeC0022735
- klinefelter's syndromesC0022735
- klinefelters syndromeC0022735
- primary hypogonadismC0022735
- xxy syndromeC0022735
Frequently Asked Questions
What is ICD-10 code Q98.0?
ICD-10-CM code Q98.0 represents "Klinefelter syndrome karyotype 47, XXY". It is a billable/specific code that can be used on a claim.
Is Q98.0 a billable code?
Yes, Q98.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q98.0 in?
Q98.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q98.0 map to?
Q98.0 maps to 7 SNOMED CT concepts: 22053006, 405769009, 205698004, 74398009, 205709009, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q98.0?
Q98.0 is linked to 1 UMLS Concept Unique Identifier: C0022735. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.