Valid for Submission
Q55.29 is a billable diagnosis code used to specify a medical diagnosis of other congenital malformations of testis and scrotum. The code Q55.29 is valid during the fiscal year 2022 from October 01, 2021 through September 30, 2022 for the submission of HIPAA-covered transactions.
The ICD-10-CM code Q55.29 might also be used to specify conditions or terms like absent scrotum, bifid scrotum, congenital abnormal shape of testis, congenital abnormality of scrotum, congenital abnormality of scrotum , congenital anomaly of endocrine testis, etc. The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals.
The code Q55.29 is applicable to male patients only. It is clinically and virtually impossible to use this code on a non-male patient.
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code Q55.29 are found in the index:
- - Anomaly, anomalous (congenital) (unspecified type) - Q89.9
- - Appendix, appendicular - See Also: condition;
- - Cyst (colloid) (mucous) (simple) (retention)
- - Malformation (congenital) - See Also: Anomaly;
The Medicare Code Editor (MCE) detects and reports errors in the coding of claims data. The following ICD-10 Code Edits are applicable to this code:
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Absent scrotum
- Bifid scrotum
- Congenital abnormal shape of testis
- Congenital abnormality of scrotum
- Congenital abnormality of scrotum
- Congenital anomaly of endocrine testis
- Congenital aplasia of scrotum
- Congenital hypertrophy of testis
- Congenital hypoplasia of gonad
- Congenital hypoplasia of testis
- Congenital malposition of testis
- Cyst of paramesonephric duct
- Cyst of testis
- Cystic testicular dysplasia
- Dead - sudden death
- Dysplasia of testis
- Hypertrophy of testis
- Leydig cell agenesis
- Mullerian remnant
- Sudden infant death syndrome
- Sudden infant death with dysgenesis of testes syndrome
- Testicular dysgenesis syndrome
- X-linked intellectual disability, macrocephaly, macroorchidism syndrome
Diagnostic Related Groups - MS-DRG Mapping
|MS-DRG||MS-DRG Title||MCD||Relative Weight|
|729||OTHER MALE REPRODUCTIVE SYSTEM DIAGNOSES WITH CC/MCC||12||1.0048|
|730||OTHER MALE REPRODUCTIVE SYSTEM DIAGNOSES WITHOUT CC/MCC||12||0.5657|
The relative weight of a diagnostic related group determines the reimbursement rate based on the severity of a patient's illness and the associated cost of care during hospitalization.
Present on Admission (POA)
Convert Q55.29 to ICD-9 Code
The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code Q55.29 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.
Information for Patients
Testicles, or testes, make male hormones and sperm. They are two egg-shaped organs inside the scrotum, the loose sac of skin behind the penis. It's easy to injure your testicles because they are not protected by bones or muscles. Men and boys should wear athletic supporters when they play sports.
You should examine your testicles monthly and seek medical attention for lumps, redness, pain or other changes. Testicles can get inflamed or infected. They can also develop cancer. Testicular cancer is rare and highly treatable. It usually happens between the ages of 15 and 40.
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