Q96.1
BillableKaryotype 46, X iso (Xq)
Karyotype 46, X iso (Xq)
Status
Billable / Specific
Parent Code
Q96Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Karyotype 46, isochromosome Xq
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- Noonan syndrome (Q87.19)
Also Known As / Clinical Terms
SNOMED CT
Frequently Asked Questions
What is the ICD-10 code for karyotype 46, x iso (xq)?
The ICD-10-CM code for karyotype 46, x iso (xq) is Q96.1. The full clinical description is "Karyotype 46, X iso (Xq)". Q96.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q96.1 mean?
ICD-10-CM code Q96.1 represents "Karyotype 46, X iso (Xq)". 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 Q96.1 a billable code?
Yes, Q96.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q96.1 in?
Q96.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q96.1?
Q96.1 has Excludes1 notes indicating codes that cannot be used together with it, including: Noonan syndrome (Q87.19).
What SNOMED CT codes does Q96.1 map to?
Q96.1 maps to 2 SNOMED CT concepts: 38804009, 205686009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q96.1?
Q96.1 is linked to 2 UMLS Concept Unique Identifiers: C0432463, C2910375. 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.