Diagnosis Code: Q52.9

Short Description: Congenital malformation of female genitalia, unspecified

Long Description: Congenital malformation of female genitalia, unspecified

The code Q52.9 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of genital organs (Q50-Q56)
    • Other congenital malformations of female genitalia (Q52)
      • Q52.9 Congenital malformation of female genitalia, unspecified

This code is valid for diagnoses for females only

Code Version: 2022 ICD-10-CM

Synonyms

• 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 testosterone and/or testosterone derivative
• 46,XX disorder of sex development due to synthetic oral progestogen
• 46,XY disorder of sex development
• Absent radius, anogenital anomalies syndrome
• Acrocardiofacial syndrome
• Agenesis of corpus callosum and abnormal genitalia syndrome
• Anal atresia
• Anal atresia
• Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
• Arachnodactyly
• Autosomal recessive facio-digito-genital syndrome
• B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome
• Cervical, vaginal and external female genital anomalies
• Congenital absence of radius
• Congenital agammaglobulinemia
• 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

Diagnostic Related Group(s)

The code Q52.9 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Uterine And Adnexa Procedures For Non-malignancy With Cc/mcc (742)
• Uterine And Adnexa Procedures For Non-malignancy Without Cc/mcc (743)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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