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Q97.8

Billable

Oth sex chromosome abnormalities, female phenotype

Other specified sex chromosome abnormalities, female phenotype

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(5)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(42)

Clinical Terms

  • Sex phenotype-karyotype dissociation syndrome
  • Giant
  • Normal giant
  • Infantile gigantism due to pituitary hyperplasia
  • Pituitary gigantism
  • Acromegalic gigantism
  • Distal trisomy Xq28
  • Absence of sex chromosome
  • Hypersomatotropic gigantism
  • Chromosome Xq26 microduplication syndrome
  • Giantism
  • Gigantism
  • Primordial giant
  • Familial infantile gigantism
  • X-linked acrogigantism due to Xq26 microduplication
  • Hereditary infantile gigantism
  • Launois syndrome
  • Genetic giant
  • Distal Xq28 microduplication syndrome
  • X-LAG (X-linked acrogigantism) due to Xq26 microduplication
Frequently Asked Questions
What is the ICD-10 code for oth sex chromosome abnormalities, female phenotype?

The ICD-10-CM code for oth sex chromosome abnormalities, female phenotype is Q97.8. The full clinical description is "Other specified sex chromosome abnormalities, female phenotype". Q97.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q97.8 mean?

ICD-10-CM code Q97.8 represents “Other specified sex chromosome abnormalities, female phenotype”. 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 Q97.8 a billable code?

Yes, Q97.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q97.8 in?

Q97.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q97.8?

Q97.8 has Excludes1 notes indicating codes that cannot be used together with it, including: Turner's syndrome (Q96.-).

What SNOMED CT codes does Q97.8 map to?

Q97.8 maps to 7 SNOMED CT concepts: 254259001, 86073008, 789187001, 773670004, 773645004, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q97.8?

Q97.8 is linked to 1 UMLS Concept Unique Identifier: C0478104. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q97.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth sex chromosome abnormalities, female phenotype affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q97.8?

Q97.8 maps to the ICD-11 code: LD5Z (Sex chromosome anomalies, unspecified).

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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.