| autosomaal dominante epilepsie met auditieve verschijnselen (aandoening) | | autosomaal dominante epilepsie met auditieve verschijnselen | | Familial epilepsy with auditory features | | Autosomal dominant lateral temporal lobe epilepsy
FEAF - familial epilepsy with auditory features
Autosomal dominant epilepsy with auditory features
| | A rare, genetic, familial partial epilepsy disease characterized by focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution. |
| | Id | 784377008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G40.1 | | Term | Lokalisatiegebonden (focale)(partiële) symptomatische epilepsie en epileptische syndromen met eenvoudige partiële aanvallen |
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| SNOMED CT to Orphanet simple map | 101046 |
| SNOMED CT to ICD-10 extended map | | Target | G40.0 | | Rule | TRUE | | Advice | ALWAYS G40.0 | 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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