Q52.8
BillableOther specified congenital malformations of female genitalia
Other specified congenital malformations of female genitalia
Status
Billable / Specific
Parent Code
Q52Coding 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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Persistent urogenital sinus11378000
- Splenogonadal fusion62042001
- Accessory gonad91845007
- Supernumerary gonad91845007
- Congenital absence of genital tubercle92967005
- Congenital hypoplasia of genital tubercle93260007
- Congenital small genital tubercle93260007
- Congenital anomaly of perineum126763008
- Congenital aplasia of round ligament204905003
- Aplasia of Müllerian ducts253828000
- Mullerian aplasia253828000
- Müllerian duct failure253828000
- Duplication of external genitalia253840000
- Mullerian remnant264491001
- Hereditary disorder of lymphatic system363190001
- Biason-Lauber syndrome699275001
- Mayer-Rokitansky-Küster-Hausel like syndrome699275001
- WNT4 Mullerian aplasia and ovarian dysfunction699275001
- WNT4 Müllerian aplasia and ovarian dysfunction699275001
- WNT4 protein deficiency699275001
- Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation702407009
- McKusick Kaufman syndrome702407009
- Haspeslagh Fryns Muelenaere syndrome716090004
- Short stature with craniofacial anomalies and genital hypoplasia syndrome716090004
- Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome721970009
- Congenital perineal groove722860006
- SERKAL (sex reversion, kidney, adrenal and lung dysgenesis) syndrome723720008
- SERKAL syndrome723720008
- Sex reversion, kidney, adrenal and lung dysgenesis syndrome723720008
- SGFLD (splenogonadal fusion limb defect syndrome) syndrome726724005
- Splenogonadal fusion limb defect syndrome726724005
- Splenogonadal fusion, limb defect, micrognathia syndrome726724005
- Congenital cyst of female genital structure767615004
- Embryonic cyst of female genital structure767615004
- Congenital lymphangiectases788292004
- Congenital lymphangiectasia788292004
- Congenital lymphangiectasis788292004
Frequently Asked Questions
What is the ICD-10 code for other specified congenital malformations of female genitalia?
The ICD-10-CM code for other specified congenital malformations of female genitalia is Q52.8. The full clinical description is "Other specified congenital malformations of female genitalia". Q52.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q52.8 mean?
ICD-10-CM code Q52.8 represents "Other specified congenital malformations of female genitalia". 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 Q52.8 a billable code?
Yes, Q52.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q52.8 in?
Q52.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q52.8?
Q52.8 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 Q52.8 map to?
Q52.8 maps to 20 SNOMED CT concepts: 91845007, 253828000, 699275001, 92967005, 126763008, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q52.8?
Q52.8 is linked to 1 UMLS Concept Unique Identifier: C0478048. 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.