Q55.29
BillableOther congenital malformations of testis and scrotum
Other congenital malformations of testis and scrotum
Status
Billable / Specific
Parent Code
Q55.2Coding 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(4)
Also Known As / Clinical Terms(99)
SNOMED CT
- Hypertrophy of testis32121007
- Cot death51178009
- Crib death51178009
- SIDS - sudden infant death syndrome51178009
- Sudden infant death syndrome51178009
- Unexpected sudden death of infant51178009
- Gonadotrophin unresponsiveness syndrome56212008
- Gonadotropin unresponsiveness syndrome56212008
- Leydig cell agenesis56212008
- Leydig cell dysgenesis56212008
- Leydig cell hypoplasia56212008
- Congenital hypoplasia of testis85437001
- Congenital micro-orchidia85437001
- Congenital micro-orchidism85437001
- Congenital small testis85437001
- Streak testis85437001
- Congenital abnormal shape of testis92952006
- Congenital misshapen testis92952006
- Congenital enlarged testis93077001
- Congenital hypertrophy of testis93077001
- Congenital hypoplasia of gonad93261006
- Congenital small gonad93261006
- Congenital malposition of testis93358007
- Congenital malpositioned testis93358007
- Cystic testicular dysplasia109560004
- Congenital aplasia of scrotum204907006
- Congenital abnormality of scrotum236779000
- Congenital anomaly of scrotum236779000
- Bifid scrotum236780002
- Absent scrotum249233008
- Mullerian remnant264491001
- Congenital anomaly of endocrine testis371122009
- Dead - sudden death418362005
- Testicular dysgenesis syndrome445338005
- Dysplasia of testis445390001
- Sudden infant death with dysgenesis of testes syndrome711157000
- Johnson syndrome719825000
- X-linked intellectual disability, macrocephaly, macroorchidism syndrome719825000
- Cyst of Mullerian duct721812005
- Cyst of Müllerian duct721812005
- Cyst of paramesonephric duct721812005
- Cyst of testis767754009
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome1172594000
- Agenesis of scrotum1187130004
- Complete absence of scrotum1187130004
- Congenital scrotal agenesis1187130004
- Congenital hypoplasia of testis and scrotum15965901000119108
Clinical Terms
- Leydig cell hypoplasia
- Congenital small testis
- Congenital misshapen testis
- Congenital abnormal shape of testis
- Agenesis of scrotum
- SIDS - sudden infant death syndrome
- Cyst of paramesonephric duct
- Gonadotropin unresponsiveness syndrome
- Congenital hypoplasia of testis and scrotum
- Congenital scrotal agenesis
- Sudden infant death syndrome
- Unexpected sudden death of infant
- X-linked intellectual disability, macrocephaly, macroorchidism syndrome
- Cyst of Mullerian duct
- Complete absence of scrotum
- Congenital hypoplasia of testis
- Congenital micro-orchidia
- Leydig cell dysgenesis
- Congenital abnormality of scrotum
- Congenital hypoplasia of gonad
- Cystic testicular dysplasia
- Congenital micro-orchidism
- Cyst of Müllerian duct
- Dysplasia of testis
- Absent scrotum
- Congenital small gonad
- Dead - sudden death
- Leydig cell agenesis
- Gonadotrophin unresponsiveness syndrome
- Cyst of testis
- Mullerian remnant
- Congenital hypertrophy of testis
- Streak testis
- Testicular dysgenesis syndrome
- Congenital anomaly of endocrine testis
- Johnson syndrome
- Hypertrophy of testis
- Congenital malposition of testis
- Congenital enlarged testis
- Congenital aplasia of scrotum
- Congenital dystrophy of cornea
- Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
- Congenital malpositioned testis
- Bifid scrotum
- Crib death
- Sudden infant death with dysgenesis of testes syndrome
- Congenital anomaly of scrotum
- Congenital corneal dystrophy
- Cot death
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of testis and scrotum?
The ICD-10-CM code for other congenital malformations of testis and scrotum is Q55.29. The full clinical description is "Other congenital malformations of testis and scrotum". Q55.29 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q55.29 mean?
ICD-10-CM code Q55.29 represents “Other congenital malformations 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 Q55.29 a billable code?
Yes, Q55.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q55.29 in?
Q55.29 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q55.29?
Q55.29 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 Q55.29 map to?
Q55.29 maps to 26 SNOMED CT concepts: 249233008, 1187130004, 236780002, 92952006, 236779000, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q55.29?
Q55.29 is linked to 1 UMLS Concept Unique Identifier: C0478050. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q55.29 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations 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 Q55.29?
There is no direct ICD-11 mapping available for Q55.29 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.