2026 ICD-10-CM Diagnosis Code Q52.9Congenital malformation of female genitalia, unspecified

ICD-10-CM Codes›Q00-Q99›Q50-Q56›Q52

ICD-10-CM Q52.9
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

Q52.9 is a billable ICD-10-CM diagnosis code for congenital malformation of female genitalia, unspecified. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 742 through 743, 760 through 761. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Genitourinary congenital anomalies.

Code Identity

ICD-10-CM Code
Q52.9
Billable Status
Yes — Valid for Submission
Code Describes
Congenital malformation of female genitalia, unspecified
Short Description
Congenital malformation of female genitalia, unspecified
Same as the full description in the CMS dataset.
Parent Code
Q52
Other congenital malformations of female genitalia

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ50-Q56Congenital malformations of genital organs
CategoryQ52Other congenital malformations of female genitalia
This CodeQ52.9Congenital malformation of female genitalia, unspecified

Present on Admission (POA)Billing

Q52.9 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • 11p partial monosomy syndrome
  • 46,XX androgen-induced disorder of sex development due to maternal adrenal hyperplasia
  • 46,XX androgen-induced disorder of sex development of iatrogenic maternal origin
  • 46,XX disorder of sex development
  • 46,XX disorder of sex development caused by synthetic oral diethylstilbestrol
  • 46,XX disorder of sex development caused by synthetic oral progestogen
  • 46,XX disorder of sex development caused by testosterone and/or testosterone derivative
  • Absent radius, anogenital anomalies syndrome
  • Acrocardiofacial syndrome
  • Agenesis of corpus callosum and abnormal genitalia syndrome
  • Anal atresia
  • Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
  • Aplasia of bone of radius and/or ulna
  • Aplasia of radius
  • Arachnodactyly
  • Autosomal recessive facio-digito-genital syndrome
  • B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome
  • Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome
  • Cardiac urogenital syndrome
  • Cervical, vaginal and external female genital anomalies
  • Congenital absence of radius
  • Congenital anomaly of female genital system
  • Congenital cleft hand
  • Congenital female urogenital anomaly
  • Congenital hypoplasia of adrenal gland
  • Congenital malformation of genital organs
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
  • Deletion of part of chromosome 11
  • Disorder of sex development with intellectual disability syndrome
  • Dysmorphism, short stature, deafness, disorder of sex development syndrome
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia with alopecia and genital anomaly syndrome
  • Genitopatellar syndrome
  • Genitourinary congenital anomalies
  • Hand-foot-genital syndrome
  • Harrod syndrome
  • Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome
  • Lethal hemolytic anemia and genital anomaly syndrome
  • MIRAGE syndrome
  • PELVIS syndrome
  • RAB18 deficiency
  • Short stature co-occurrent and due to endocrine disorder
  • Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome
  • STAR syndrome
  • Telecanthus
  • Urban Rogers Meyer syndrome
  • WAGR syndrome
  • X-linked lissencephaly with abnormal genitalia syndrome

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Anomaly, anomalous(congenital) (unspecified type)
      • genitalia, genital organ (s) or system
        • female
    • Anomaly, anomalous(congenital) (unspecified type)
      • genitalia, genital organ (s) or system
        • female
          • internal NOS
    • Anomaly, anomalous(congenital) (unspecified type)
      • genitourinary NEC
        • female
    • Deformity
      • genitalia, genital organ (s) or system NEC
        • female (congenital)

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR MAL003
Genitourinary congenital anomalies
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Arachnodactyly

    an abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar side of the hand. arachnodactyly can include feet and toes. arachnodactyly has been associated with several gene mutations and syndromes.

  • WAGR Syndrome

    a contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. the condition is marked by the combination of wilms tumor; aniridia; genitourinary abnormalities; and intellectual disability.

Patient EducationClinical

Birth Defects

A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.

The full article covers:

  • What are birth defects?
  • What causes birth defects?
  • Who is at risk of having a baby with birth defects?
  • How are birth defects diagnosed?
  • What are the treatments for birth defects?
  • Can birth defects be prevented?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert Q52.9 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
752.40 Cervix/fem gen anom NOS
Approximate The match is approximate rather than exact.
ICD-9-CM
752.9 Genital organ anom NOS
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About Q52.9Overview

Is Q52.9 (Other congenital malformations of female genitalia) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report congenital malformation of female genitalia, unspecified on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does Q52.9 group to?

When congenital malformation of female genitalia, unspecified is the principal diagnosis on an inpatient stay, it groups to MS-DRG 742, 743, 760, 761, with relative weights from 0.5696 to 1.8348 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q52.9 exempt from POA reporting?

Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for congenital malformation of female genitalia, unspecified on inpatient claims.

What is the ICD-9 equivalent of Q52.9?

Under the General Equivalence Mappings, congenital malformation of female genitalia, unspecified converts to ICD-9-CM 752.40 (cervix/fem gen anom NOS) and 752.9 (genital organ anom NOS). The mapping is approximate, so confirm the match fits the documentation.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.