Q97.8
BillableOth sex chromosome abnormalities, female phenotype
Other specified sex chromosome abnormalities, female phenotype
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(42)
SNOMED CT
- Sex phenotype-karyotype dissociation syndrome36114005
- Genetic giant80849007
- Giant80849007
- Giantism80849007
- Gigantism80849007
- Normal giant80849007
- Primordial giant80849007
- Acromegalic gigantism86073008
- Hypersomatotropic gigantism86073008
- Launois syndrome86073008
- Pituitary gigantism86073008
- Absence of sex chromosome254259001
- Familial infantile gigantism773645004
- Hereditary infantile gigantism773645004
- Infantile gigantism due to pituitary hyperplasia773645004
- Distal Xq28 microduplication syndrome773670004
- Distal trisomy Xq28773670004
- Chromosome Xq26 microduplication syndrome789187001
- X-LAG (X-linked acrogigantism) due to Xq26 microduplication789187001
- X-linked acrogigantism due to Xq26 microduplication789187001
UMLS
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.