Q50.02
BillableCongenital absence of ovary, bilateral
Congenital absence of ovary, bilateral
Status
Billable / Specific
Parent Code
Q50.0Coding 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(1)
Also Known As / Clinical Terms(21)
SNOMED CT
- Congenital absence of ovary12017008
- Congenital absence of gonads92968000
- Bilateral congenital absence of ovary717703006
- Congenital absence of ovary, bilateral717703006
- PAGOD (pulmonary hypoplasia, hypoplasia pulmonary artery, agonadism, omphalocele, dextrocardia) syndrome722132007
- PAGOD syndrome722132007
- Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome722132007
- Congenital anomaly of left ovary15932341000119105
- Congenital anomaly of right ovary15932301000119108
UMLS
Clinical Terms
- Bilateral congenital absence of ovary (disorder)
- PAGOD (pulmonary hypoplasia, hypoplasia pulmonary artery, agonadism, omphalocele, dextrocardia) syndrome
- Bilateral congenital absence of ovary
- PAGOD syndrome
- Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome
- Congenital absence of gonads
- Congenital absence of ovary
- Congenital anomaly of left ovary
- Congenital anomaly of right ovary
Frequently Asked Questions
What is the ICD-10 code for congenital absence of ovary, bilateral?
The ICD-10-CM code for congenital absence of ovary, bilateral is Q50.02. The full clinical description is "Congenital absence of ovary, bilateral". Q50.02 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q50.02 mean?
ICD-10-CM code Q50.02 represents “Congenital absence of ovary, bilateral”. 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 Q50.02 a billable code?
Yes, Q50.02 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q50.02 in?
Q50.02 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q50.02?
Q50.02 has Excludes1 notes indicating codes that cannot be used together with it, including: androgen insensitivity syndrome (E34.5-); syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99); Turner's syndrome (Q96.-).
What SNOMED CT codes does Q50.02 map to?
Q50.02 maps to 6 SNOMED CT concepts: 717703006, 92968000, 12017008, 15932341000119105, 15932301000119108, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q50.02?
Q50.02 is linked to 1 UMLS Concept Unique Identifier: C2910194. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q50.02 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital absence of ovary, bilateral 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 Q50.02?
There is no direct ICD-11 mapping available for Q50.02 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.