| epitheliale corneadystrofie van Lisch (aandoening) | | epitheliale corneadystrofie van Lisch | | LECD
bandvormige en gedraaide microcystische dystrofie van hoornvliesepitheel
| | Lisch epithelial corneal dystrophy | | Band-shaped and whorled microcystic dystrophy of corneal epithelium
| | A very rare form of superficial corneal dystrophy with characteristics of feather-shaped opacities and microcysts in the corneal epithelium arranged in a band-shaped and sometimes whorled pattern, occasionally with impaired vision. Exact prevalence of this form of corneal dystrophy is not known but very few cases have been reported to date. Lesions generally develop in childhood. Epithelial opacities are slowly progressive and painless blurred vision sometimes occurs after 60 years of age. The exact cause is unknown but appears to be genetic. The gene related to Lisch epithelial corneal dystrophy has been mapped to the short arm of the X chromosome (Xp22.3). |
| | Id | 724175002 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | H18.5 | | Term | Hereditaire corneadystrofieën |
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| SNOMED CT to Orphanet simple map | 98955 |
| SNOMED CT to ICD-10 extended map | | Target | H18.5 | | Rule | TRUE | | Advice | ALWAYS H18.5 | 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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