| X-gebonden verstandelijke beperking Cantagrel-type (aandoening) | | X-gebonden verstandelijke beperking Cantagrel-type | | X-gebonden verstandelijke handicap Cantagrel-type
X-gebonden mentale retardatie Cantagrel-type
| | X-linked intellectual disability Cantagrel type | | A rare X-linked intellectual disability characterized by marked neonatal hypotonia, progressive quadriparesia, severely delayed developmental milestones (walking at 3 years of age), gastroesophageal reflux, stereotypic movements of the hands, esotropia and infantile autism. |
| | Id | 719016007 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| DHD Diagnosis thesaurus reference set |
| 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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| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.8 | | Term | Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd |
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