| familiaire geïsoleerde retinale arteriële tortuositeit (aandoening) | | familiaire geïsoleerde retinale arteriële tortuositeit | | familiaire geïsoleerde retinale bloeding met vasculaire tortuositeit
familiaire geïsoleerde tortuositas van retinale arterie
familiaire geïsoleerde hemorragie met vasculaire tortuoisiteit
| | Familial isolated retinal arterial tortuosity | | Tortuosity of retinal arteries
Retinal arteriolar tortuosity
Retinal hemorrhage with vascular tortuosity
| | A rare genetic cerebral small vessel disease with isolated marked tortuosity of second order and third order retinal arteries with normal first order arteries and venous system, typically located in the macular and peripapillary area and developing during childhood or early adulthood. The disease may be asymptomatic, although most patients present variable degrees of transient vision loss due to retinal hemorrhage following physical exertion or minor trauma. |
| | Id | 1231183003 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 75326 |
| SNOMED CT to ICD-10 extended map | | Target | H35.8 | | Rule | TRUE | | Advice | ALWAYS H35.8 | 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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