| syndroom van hallux varus en preaxiale polysyndactylie (aandoening) | | syndroom van hallux varus en preaxiale polysyndactylie | | syndroom van Kleiner-Holmes
| | Hallux varus, preaxial polysyndactyly syndrome | | Kleiner Holmes syndrome
| | A rare genetic congenital limb malformation disorder with characteristics of bilateral medial displacement of the hallux and preaxial polysyndactyly of the first toes. Radiographs show broad, shortened, misshapen first metatarsals and may associate incomplete or complete duplication of proximal phalanges and duplication or triplication of distal phalanges. There have been no further descriptions in the literature since 1980. |
| | Id | 771180005 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q74.2 | | Term | Overige congenitale misvormingen van onderste extremiteit(en), inclusief bekkengordel |
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| SNOMED CT to Orphanet simple map | 2110 |
| SNOMED CT to ICD-10 extended map | | Target | Q74.2 | | Rule | TRUE | | Advice | ALWAYS Q74.2 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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