Q64.79
BillableOther congenital malformations of bladder and urethra
Other congenital malformations of bladder and urethra
Status
Billable / Specific
Parent Code
Q64.7Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Enterovesical fistula40046003
- Intestinovesical fistula40046003
- Vesico-intestinal fistula40046003
- Vesicoenteric fistula40046003
- UVF - Urethrovaginal fistula50477003
- Urethral fistula to vagina50477003
- Urethrovaginal fistula50477003
- Bladder distension54768000
- Bladder distention54768000
- Distended bladder54768000
- Distension of urinary bladder54768000
- Accessory bladder62500006
- Accessory urinary bladder62500006
- Congenital rectovesical fistula64283009
- Rectovesical fistula68301001
- Vesicorectal fistula68301001
- Double urethra69015003
- Duplication of urethra69015003
- Cyst of urethra70795003
- Urethral cyst70795003
- Accessory urethra82635007
- Congenital cyst of bladder93046003
- Congenital cyst of urinary bladder93046003
- Congenital dilatation of bladder93052002
- Congenital dilatation of urinary bladder93052002
- Congenital distended bladder93052002
- Congenital hypoplasia of bladder93245009
- Congenital hypoplasia of urinary bladder93245009
- Congenital small bladder93245009
- Congenital hourglass bladder205024005
- Congenital hourglass urinary bladder205024005
- Rectourinary fistula235784001
- Congenital fistula of rectum253773000
- Congenital functional disorders of the colon253778009
- Berdon syndrome253781004
- Megacystis, microcolon, hypoperistalsis syndrome253781004
- Congenital urethrovaginal fistula253837000
- Congenital parameatal cyst253856005
- Congenital short urethra253903007
- Megacystis-megaureter syndrome253904001
- Megalourethra253905000
- Congenital urethral syringocele253906004
- Congenital gastrointestinal-urinary tract fistula253909006
- Partial duplication of urethra717757004
- Megalourethra of spongiose portion of urethra1003879007
- Penile megalourethra1003879007
- Dilatation of urethra1204394008
- Dilation of urethra1204394008
- Distended urethra1204394008
- Urethral distension1204394008
- Urethral parameatal cyst125991000119108
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of bladder and urethra?
The ICD-10-CM code for other congenital malformations of bladder and urethra is Q64.79. The full clinical description is "Other congenital malformations of bladder and urethra". Q64.79 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q64.79 mean?
ICD-10-CM code Q64.79 represents "Other congenital malformations of bladder and urethra". 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 Q64.79 a billable code?
Yes, Q64.79 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q64.79 in?
Q64.79 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q64.79?
Q64.79 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital prolapse of bladder (mucosa) (Q79.4).
What SNOMED CT codes does Q64.79 map to?
Q64.79 maps to 28 SNOMED CT concepts: 62500006, 82635007, 253781004, 54768000, 93046003, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q64.79?
Q64.79 is linked to 1 UMLS Concept Unique Identifier: C0478060. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.