| congenitale niet-syndromale anorectale malformatie (aandoening) | | congenitale niet-syndromale anorectale malformatie | | aangeboren niet-syndromale anorectale misvorming
geïsoleerde congenitale anorectale malformatie
| | Congenital non-syndromic anorectal malformation | | Non-syndromic ARM (anorectal malformation)
Non-syndromic anorectal malformation
| | A wide spectrum of malformations involving the distal anus and rectum along with urinary and genital tracts, which can affect male or female. Defects range from mild anal anomalies to complex cloacal malformations. They can therefore be classified into the following groups: imperforated anus without fistula, ARM with rectourinary or rectogenital fistula and complex ARM (cloaca). Associated anomalies include genitourinary defects in approximately 50% of patients and spinal anomalies. The etiology remains unclear and is likely multifactorial. Familial cases have been described. |
| | Id | 1264114007 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 557 |
| SNOMED CT to ICD-10 extended map | | Target | Q43.9 | | Rule | TRUE | | Advice | ALWAYS Q43.9 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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