AutoICD API

Q98.5

Billable

Karyotype 47, XYY

Karyotype 47, XYY

Status

Billable / Specific

Parent Code

Q98

Coding Notes

Excludes 2

Conditions not included here, but the patient may have both

  • inborn errors of metabolism (E70-E88)
  • mitochondrial metabolic disorders (E88.4-)

Also Known As / Clinical Terms

SNOMED CT

UMLS

Frequently Asked Questions

What is the ICD-10 code for karyotype 47, xyy?

The ICD-10-CM code for karyotype 47, xyy is Q98.5. The full clinical description is "Karyotype 47, XYY". Q98.5 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q98.5 mean?

ICD-10-CM code Q98.5 represents "Karyotype 47, XYY". 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 Q98.5 a billable code?

Yes, Q98.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q98.5 in?

Q98.5 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q98.5 map to?

Q98.5 maps to 2 SNOMED CT concepts: 50749006, 725084009. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q98.5?

Q98.5 is linked to 1 UMLS Concept Unique Identifier: C0043379. 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.