Q55.1
BillableHypoplasia of testis and scrotum
Hypoplasia of testis and scrotum
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Fusion of testes
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
Q55.2Oth 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
Q55.8Oth congenital malformations of male genital organs
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(68)
SNOMED CT
- Congenital fusion of testis44964000
- Fusion of testes44964000
- Synorchism44964000
- Testicular regression - embryonic53599007
- Testicular regression syndrome53599007
- Vanishing testes syndrome53599007
- XY Gonadal agenesis syndrome53599007
- Gonadotrophin unresponsiveness syndrome56212008
- Gonadotropin unresponsiveness syndrome56212008
- Leydig cell agenesis56212008
- Leydig cell dysgenesis56212008
- Leydig cell hypoplasia56212008
- Streak gonad84814009
- Congenital hypoplasia of testis85437001
- Congenital micro-orchidia85437001
- Congenital micro-orchidism85437001
- Congenital small testis85437001
- Streak testis85437001
- Congenital hypoplasia of gonad93261006
- Congenital small gonad93261006
- Hypoplasia of scrotum204912007
- Male infertility of developmental origin236794001
- Congenital anomaly of endocrine testis371122009
- Infertility due to testicular hypoplasia414494005
- Leydig cell hypoplasia due to complete LH receptor inactivation1003437009
- Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation1003437009
- Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation1003437009
- Leydig cell hypoplasia due to partial LH receptor inactivation1003438004
- Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation1003438004
- Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation1003438004
- Congenital hypoplasia of testis and scrotum15965901000119108
UMLS
Clinical Terms
- Leydig cell hypoplasia
- Congenital small testis
- Synorchism
- Gonadotropin unresponsiveness syndrome
- Congenital hypoplasia of testis and scrotum
- Leydig cell hypoplasia due to complete LH receptor inactivation
- XY Gonadal agenesis syndrome
- Congenital hypoplasia of testis
- Congenital micro-orchidia
- Infertility due to testicular hypoplasia
- Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation
- Testicular regression - embryonic
- Leydig cell dysgenesis
- Testicular regression syndrome
- Congenital hypoplasia of gonad
- Congenital micro-orchidism
- Congenital small gonad
- Leydig cell hypoplasia due to partial LH receptor inactivation
- Congenital fusion of testis (disorder)
- Leydig cell agenesis
- Gonadotrophin unresponsiveness syndrome
- Vanishing testes syndrome
- Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
- Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation
- Streak testis
- Congenital anomaly of endocrine testis
- Streak gonad
- Congenital fusion of testis
- Male infertility of developmental origin
- Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
- Fusion of testes
- Hypoplasia of scrotum
Frequently Asked Questions
What is the ICD-10 code for hypoplasia of testis and scrotum?
The ICD-10-CM code for hypoplasia of testis and scrotum is Q55.1. The full clinical description is "Hypoplasia of testis and scrotum". Q55.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q55.1 mean?
ICD-10-CM code Q55.1 represents “Hypoplasia of testis and scrotum”. 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 Q55.1 a billable code?
Yes, Q55.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q55.1 in?
Q55.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q55.1?
Q55.1 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 Q55.1 map to?
Q55.1 maps to 13 SNOMED CT concepts: 371122009, 44964000, 93261006, 85437001, 15965901000119108, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q55.1?
Q55.1 is linked to 2 UMLS Concept Unique Identifiers: C0266428, C0495574. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q55.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypoplasia of testis and scrotum 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 Q55.1?
Q55.1 maps to the ICD-11 code: LB59 (Hypoplasia of testis or scrotum).
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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.