| spermine synthase deficiency (aandoening) | | spermine synthase deficiency | | syndroom van Snyder-Robinson
| | Snyder-Robinson syndrome | | Mental retardation, x-linked, Snyder-Robinson type
Snyder-Robinson x-linked mental retardation syndrome
X-linked intellectual disability Snyder type
|
| | Id | 702416008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.8 | | Term | Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd |
| Target | F71.9 | | Term | Matige zwakzinnigheid [imbeciliteit]; Zonder vermelding van gedragsstoornissen |
|
| SNOMED CT to Orphanet simple map | 3063 |
| SNOMED CT to ICD-10 extended map | | Target | F88 | | Rule | TRUE | | Advice | ALWAYS F88 | 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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