| syndroom van syndactylie, camptodactylie en clinodactylie van digitus V van hand en gespleten digiti van voet (aandoening) | | syndroom van syndactylie, camptodactylie en clinodactylie van digitus V van hand en gespleten digiti van voet | | syndroom van Wahab
syndroom van syndactylie, camptodactylie en clinodactylie van pink en gespleten tenen
| | Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome | | Synactyly, camptodactyly and clinodactyly of fifth fingers, bifid halluces syndrome
Wahab syndrome
| | A rare genetic congenital limb malformation syndrome with characteristics of a unique combination of bilateral, symmetrical camptodactyly and clinodactyly of fifth fingers, mesoaxial camptodactyly of toes and ulnar deviation of third fingers. Additional variable manifestations include bifid toes and severe syndactyly or synpolydactyly involving all digits of hands and feet. |
| | Id | 783553008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.2 | | Term | Congenitale gestoorde-ontwikkelingssyndromen van hoofdzakelijk extremiteiten |
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| SNOMED CT to Orphanet simple map | 357332 |
| SNOMED CT to ICD-10 extended map | | Target | Q87.2 | | Rule | TRUE | | Advice | ALWAYS Q87.2 | 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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