Diagnosis Code: Q55.9

Short Description: Congenital malformation of male genital organ, unspecified

Long Description: Congenital malformation of male genital organ, unspecified

The code Q55.9 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 male genital organs (Q55)
      • Q55.9 Congenital malformation of male genital organ, unspecified

This code is valid for diagnoses for males only

Code Version: 2022 ICD-10-CM

Synonyms

• 11p partial monosomy syndrome
• 46,XY disorder of sex development
• 46,XY disorder of sex development
• 46,XY disorder of sex development
• 46,XY disorder of sex development
• 46,XY disorder of sex development
• 46,XY disorder of sex development due to environmental chemical exposure
• 46,XY disorder of sex development due to isolated 17,20-lyase deficiency
• 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
• Congenital absence of radius
• Congenital agammaglobulinemia
• Congenital anomaly of male genital system
• Congenital anomaly of male urogenital tract
• Congenital cleft hand
• Congenital hypoplasia of adrenal gland
• Congenital malformation of genital organs
• Congenital obstructive azoospermia
• 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
• McKusick Kaufman syndrome
• MIRAGE syndrome
• Myotubular myopathy
• 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
• X-linked myotubular myopathy, abnormal genitalia syndrome

Diagnostic Related Group(s)

The code Q55.9 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Male Reproductive System Diagnoses With Cc/mcc (729)
• Other Male Reproductive System Diagnoses Without Cc/mcc (730)

References to Index of Diseases and Injuries

The code Q55.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital anomaly of male genital organ
  • Congenital deformity of male genital organ

Crosswalk Information

Similar Codes

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

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