| primaire desmosis coli (aandoening) | | primaire desmosis coli | | Primary desmosis coli | | Aplastic desmosis coli
| | A rare intestinal disease with characteristics of congenital partial or complete lack of the collagen mesh network in the intestinal wall resulting in hypoperistalsis or aperistalsis. The enteric nervous system is normal or near normal in the affected areas, although hypo and dysganglionosis may be found in some proximal segments of the colon and/or small bowel. Patients present with chronic intractable slow transit constipation. |
| | Id | 1222675000 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 565641 |
| SNOMED CT to ICD-10 extended map | | Target | K59.8 | | Rule | TRUE | | Advice | ALWAYS K59.8 | 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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