Q55.8
BillableOth congenital malformations of male genital organs
Other specified congenital malformations of male genital organs
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)
Q55.0Absence and aplasia of testis
Q55.1Hypoplasia of testis and scrotum
Q55.2Oth and unsp congenital malformations of testis and scrotum
Q55.3Atresia of vas deferens
Q55.4Oth congen malform of vas def,epidid, semnl vescl & prostate
Q55.5Congenital absence and aplasia of penis
Q55.6Other congenital malformations of penis
Q55.7Congenital vasocutaneous fistula
Q55.9Congenital malformation of male genital organ, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(60)
SNOMED CT
- Splenogonadal fusion62042001
- Accessory gonad91845007
- Supernumerary gonad91845007
- Congenital absence of genital tubercle92967005
- Congenital hypoplasia of genital tubercle93260007
- Congenital small genital tubercle93260007
- Increased anogenital distance93613008
- Congenital anomaly of perineum126763008
- Mullerian remnant264491001
- Hereditary disorder of lymphatic system363190001
- Congenital penile adhesion699871003
- 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
- Embryonic cyst of male genital structure767641005
- Genitoperineal raphe cyst782194002
- Median raphe cyst782194002
- Congenital lymphangiectases788292004
- Congenital lymphangiectasia788292004
- Congenital lymphangiectasis788292004
- Congenital hypoplasia of external genitalia1144390001
- Congenital hypoplasia of male external genitalia1144863004
UMLS
Clinical Terms
- Congenital hypoplasia of male external genitalia
- Supernumerary gonad
- 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
- Genitoperineal raphe cyst
- Congenital absence of genital tubercle
- Congenital hypoplasia of external genitalia
- Median raphe cyst
- Short stature with craniofacial anomalies and genital hypoplasia syndrome
- Hereditary disorder of lymphatic system
- Congenital lymphangiectasia
- Congenital penile adhesion
- Sex reversion, kidney, adrenal and lung dysgenesis syndrome
- Splenogonadal fusion limb defect syndrome
- Congenital lymphangiectases
- Congenital hypoplasia of genital tubercle
- Mullerian remnant
- Accessory gonad
- Embryonic cyst of male genital structure
- Increased anogenital distance
- Splenogonadal fusion, limb defect, micrognathia syndrome
- SERKAL syndrome
- Haspeslagh Fryns Muelenaere syndrome
- Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome
Frequently Asked Questions
What is the ICD-10 code for oth congenital malformations of male genital organs?
The ICD-10-CM code for oth congenital malformations of male genital organs is Q55.8. The full clinical description is "Other specified congenital malformations of male genital organs". Q55.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q55.8 mean?
ICD-10-CM code Q55.8 represents “Other specified congenital malformations of male genital organs”. 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 Q55.8 a billable code?
Yes, Q55.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q55.8 in?
Q55.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q55.8?
Q55.8 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); congenital hydrocele (P83.5); and 1 more.
What SNOMED CT codes does Q55.8 map to?
Q55.8 maps to 19 SNOMED CT concepts: 91845007, 92967005, 126763008, 1144390001, 93260007, and 14 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q55.8?
Q55.8 is linked to 1 UMLS Concept Unique Identifier: C0478053. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q55.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth congenital malformations of male genital organs 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 Q55.8?
Q55.8 maps to the ICD-11 code: LB5Z (Structural developmental anomalies of the male genital system, 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.