Q50.39
BillableOther congenital malformation of ovary
Other congenital malformation of ovary
Status
Billable / Specific
Parent Code
Q50.3Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital malformation of ovary NOS
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(2)
Also Known As / Clinical Terms(75)
SNOMED CT
- Congenital absence of ovary12017008
- Anomalies of ovaries38296007
- Congenital anomaly of ovary38296007
- Ectopic ovary62524003
- Large ovary66998000
- Ovarian enlargement66998000
- Congenital abnormal shape of ovary92932005
- Congenital misshapen ovary92932005
- Congenital enlarged ovary93073002
- Congenital hypertrophy of ovary93073002
- Congenital hypoplasia of gonad93261006
- Congenital small gonad93261006
- Congenital hypoplasia of ovary93279005
- Congenital small ovary93279005
- Congenital malposition of ovary93341002
- Congenital malpositioned ovary93341002
- Epoophoron263993001
- Congenital anomalies of ovaries and fallopian tubes271961001
- Congenital malformation of ovaries and fallopian tubes271961001
- Duct of epoophoron279920004
- Vesicular appendix of ovary279921000
- Small ovary289837004
- Dysplastic ovary360424008
- Congenital ovarian dysplasia360426005
- Finding of size of ovary366315007
- Size of ovary - finding366315007
- Congenital anomaly of endocrine ovary370966000
- Hypertrophy of ovary441981006
- Aplasia of ovary1144554007
- Congenital anomaly of left ovary15932341000119105
- Congenital anomaly of right ovary15932301000119108
UMLS
- Anomalies of ovariesC0158688
- Congenital anomaly of ovaryC0158688
- Congenital anomaly of ovary (disorder)C0158688
- Congenital malformation of ovary NOSC0158688
- Congenital ovarian anomalyC0158688
- Congenital ovarian anomaly NOSC0158688
- Other congenital malformation of ovaryC0478042
- Other congenital malformations of ovaryC0478042
Clinical Terms
- Congenital anomaly of endocrine ovary
- Congenital anomaly of ovary (disorder)
- Other congenital malformations of ovary
- Aplasia of ovary
- Finding of size of ovary
- Congenital anomaly of right ovary
- Ovarian enlargement
- Congenital anomaly of ovary
- Congenital hypoplasia of ovary
- Duct of epoophoron
- Congenital absence of ovary
- Congenital hypoplasia of gonad
- Size of ovary - finding
- Congenital anomaly of left ovary
- Large ovary
- Congenital small gonad
- Congenital malposition of ovary
- Congenital ovarian anomaly
- Hypertrophy of ovary
- Congenital abnormal shape of ovary
- Congenital malformation of ovary NOS
- Congenital hypertrophy of ovary
- Small ovary
- Epoophoron
- Vesicular appendix of ovary
- Congenital ovarian dysplasia
- Anomalies of ovaries
- Congenital small ovary
- Congenital anomalies of ovaries and fallopian tubes
- Dysplastic ovary
- Congenital malformation of ovaries and fallopian tubes
- Congenital malpositioned ovary
- Congenital ovarian anomaly NOS
- Congenital misshapen ovary
- Congenital enlarged ovary
- Ectopic ovary
Frequently Asked Questions
What is the ICD-10 code for other congenital malformation of ovary?
The ICD-10-CM code for other congenital malformation of ovary is Q50.39. The full clinical description is "Other congenital malformation of ovary". Q50.39 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q50.39 mean?
ICD-10-CM code Q50.39 represents “Other congenital malformation of ovary”. 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 Q50.39 a billable code?
Yes, Q50.39 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q50.39 in?
Q50.39 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q50.39?
Q50.39 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).
What SNOMED CT codes does Q50.39 map to?
Q50.39 maps to 22 SNOMED CT concepts: 38296007, 1144554007, 92932005, 12017008, 271961001, and 17 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q50.39?
Q50.39 is linked to 2 UMLS Concept Unique Identifiers: C0158688, C0478042. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q50.39 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformation of ovary 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 Q50.39?
There is no direct ICD-11 mapping available for Q50.39 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.