AutoICD API

Q52.8

Billable

Other specified congenital malformations of female genitalia

Other specified congenital malformations of female genitalia

Status

Billable / Specific

Parent Code

Q52

ICD-11 Mapping

1 equivalent

Coding 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(9)
Q52.0

Congenital absence of vagina

BillableQ52.1

Doubling of vagina

Q52.2

Congenital rectovaginal fistula

BillableQ52.3

Imperforate hymen

BillableQ52.4

Other congenital malformations of vagina

BillableQ52.5

Fusion of labia

BillableQ52.6

Congenital malformation of clitoris

BillableQ52.7

Other and unspecified congenital malformations of vulva

Q52.9

Congenital malformation of female genitalia, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

KC0ZGenitourinary system disorders specific to the perinatal or neonatal period, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(75)

SNOMED CT

UMLS

Clinical Terms

  • Supernumerary gonad
  • Mayer-Rokitansky-Küster-Hausel like syndrome
  • Congenital perineal groove
  • Congenital small genital tubercle
  • Congenital lymphangiectasis
  • SGFLD (splenogonadal fusion limb defect syndrome) syndrome
  • SERKAL (sex reversion, kidney, adrenal and lung dysgenesis) syndrome
  • Splenogonadal fusion
  • Congenital anomaly of perineum
  • Congenital cyst of female genital structure
  • Congenital absence of genital tubercle
  • Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation
  • Biason-Lauber syndrome
  • Embryonic cyst of female genital structure
  • Short stature with craniofacial anomalies and genital hypoplasia syndrome
  • Hereditary disorder of lymphatic system
  • Congenital lymphangiectasia
  • Sex reversion, kidney, adrenal and lung dysgenesis syndrome
  • Splenogonadal fusion limb defect syndrome
  • WNT4 Müllerian aplasia and ovarian dysfunction
  • Congenital lymphangiectases
  • Congenital hypoplasia of genital tubercle
  • Mullerian remnant
  • Mullerian aplasia
  • Congenital aplasia of round ligament
  • WNT4 protein deficiency
  • Accessory gonad
  • Müllerian duct failure
  • WNT4 Mullerian aplasia and ovarian dysfunction
  • Aplasia of Müllerian ducts
  • Duplication of external genitalia
  • McKusick Kaufman syndrome
  • Splenogonadal fusion, limb defect, micrognathia syndrome
  • SERKAL syndrome
  • Haspeslagh Fryns Muelenaere syndrome
  • Persistent urogenital sinus
  • Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome
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.

How does Q52.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of female genitalia 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 Q52.8?

Q52.8 maps to the ICD-11 code: KC0Z (Genitourinary system disorders specific to the perinatal or neonatal period, unspecified).

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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.