Q55.4

Billable

Oth congen malform of vas def,epidid, semnl vescl & prostate

Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate

Status

Billable / Specific

Parent Code

Q55

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Absence or aplasia of prostate
  • Absence or aplasia of spermatic cord
  • Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS

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)
Q55.0

Absence and aplasia of testis

BillableQ55.1

Hypoplasia of testis and scrotum

BillableQ55.2

Oth and unsp congenital malformations of testis and scrotum

Q55.3

Atresia of vas deferens

BillableQ55.5

Congenital absence and aplasia of penis

BillableQ55.6

Other congenital malformations of penis

Q55.7

Congenital vasocutaneous fistula

BillableQ55.8

Oth congenital malformations of male genital organs

BillableQ55.9

Congenital malformation of male genital organ, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LB5ZStructural developmental anomalies of the male genital system, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(90)

SNOMED CT

UMLS

Clinical Terms

  • Agenesis of epididymis
  • Congenital absence of epididymis
  • Aplasia of spermatic cord
  • Congenital absence of vas deferens
  • Cyst of mesonephric duct
  • Congenital anomaly of vas deferens
  • Congenital anomaly of prostate
  • Cyst of hydatid of Morgagni
  • Congenital absence of seminal vesicle
  • Congenital hypoplasia of testis and scrotum
  • Absence or aplasia of prostate
  • Atresia of ejaculatory duct
  • Congenital abnormality of prostate
  • Congenital abnormality of spermatic cord
  • Congenital atresia of ejaculatory duct
  • Congenital small epididymis
  • Congenital aplasia of vas deferens
  • Congenital hypoplasia of epididymis
  • Congenital malpositioned vas deferens
  • Vas deferens absent
  • Cyst of Wolffian duct
  • Absent vasa
  • Rudimentary vas deferens
  • Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS
  • Congenital malposition of epididymis
  • Congenital bilateral aplasia of vas deferens
  • Congenital short epididymis
  • CAVD - Congenital aplasia of vas deferens
  • Hydatid cyst of Morgagni - male
  • Absence or aplasia of spermatic cord
  • Congenital absence of spermatic cord
  • Congenital hypoplasia of vas deferens
  • Observation of appearance of epididymis
  • Craggy epididymis
  • Wolffian cyst
  • Epididymis absent
  • Congenital aplasia of spermatic cord
  • Congenital anomaly of epididymis
  • Congenital absence of prostate
  • Finding of appearance of epididymis
  • Congenital malpositioned epididymis
  • Wolffian duct cyst - male
  • Congenital malposition of vas deferens
  • Congenital anomaly of spermatic cord
Frequently Asked Questions
What is the ICD-10 code for oth congen malform of vas def,epidid, semnl vescl & prostate?

The ICD-10-CM code for oth congen malform of vas def,epidid, semnl vescl & prostate is Q55.4. The full clinical description is "Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate". Q55.4 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q55.4 mean?

ICD-10-CM code Q55.4 represents “Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate”. 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 Q55.4 a billable code?

Yes, Q55.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q55.4 in?

Q55.4 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q55.4?

Q55.4 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 Q55.4 map to?

Q55.4 maps to 27 SNOMED CT concepts: 5286009, 1003575006, 702616003, 29345006, 702610009, and 22 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q55.4?

Q55.4 is linked to 4 UMLS Concept Unique Identifiers: C2910216, C2910217, C2910218, C0478051. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q55.4 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth congen malform of vas def,epidid, semnl vescl & prostate 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 Q55.4?

Q55.4 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.