Q99.1
Billable46, XX true hermaphrodite
46, XX true hermaphrodite
Status
Billable / Specific
Parent Code
Q99Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Ovarian dysgenesis with normal chromosomes95198001
- Pure gonadal dysgenesis 46,XX95198001
- Pure gonadal dysgenesis 46,XY95218005
- Swyer syndrome95218005
- Pure gonadal dysgenesis95219002
- Ovarian dysgenesis205683001
- Congenital anomaly of endocrine ovary370966000
- Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome721977007
- Gardner Silengo Wachtel syndrome773749003
- Genitopalatocardiac syndrome773749003
Frequently Asked Questions
What is ICD-10 code Q99.1?
ICD-10-CM code Q99.1 represents "46, XX true hermaphrodite". It is a billable/specific code that can be used on a claim.
Is Q99.1 a billable code?
Yes, Q99.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q99.1 in?
Q99.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q99.1 map to?
Q99.1 maps to 7 SNOMED CT concepts: 370966000, 773749003, 721977007, 205683001, 95198001, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q99.1?
Q99.1 is linked to 4 UMLS Concept Unique Identifiers: C0432481, C2910378, C2910379, C0687149. 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.