ORPHA:295004
Central polydactyly
Synonyms: Mesoaxial polydactyly
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare congenital limb malformation characterized by complete or partial duplication of one of the three middle digits in a hand or foot. It most commonly affects the fourth digit. The malformation may be unilateral or bilateral and can occur as an isolated defect or in association with other anomalies.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Central polydactyly | Mesoaxial polydactyly |
| fr | Polydactylie centrale | Polydactylie mésoaxiale |
| de | Zentrale Polydaktylie | Mesoaxiale Polydaktylie |
| es | Polidactilia central | Polidactilia en espejo · Polidactilia mesoaxial |
| it | Polidattilia centrale | Mano a specchio · Polidattilia centrale della mano · Polidattilia mesoassiale delle dita delle mani |
| nl | Centrale polydactylie | Mesoaxiale polydactylie |
| pt | Polidactilia central dos dedos da mão | Mão em espelho · Polidactilia central da mão · Polidactilia mesoaxial dos dedos da mão |
| pl | Polidaktylia centralna palców | Dłoń lustrzana · Mezoaksjalna (centralna) polidaktylia palców ręki · Polidaktylia centralna dłoni |
| cs | Centrální polydaktylie prstů ruky | Centrální polydaktylie ruky · Zrcadlová ruka · Mesoaxiální polydaktylie prstů ruky |
| uk | Центральна полідактилія | Мезоаксіальна полідактилія |
| zh | 中间指/趾畸形 | 轴间多指（趾）畸形 |
| tr | Merkezi polidaktili | Mezoaksiyel polidaktili |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q69.0 | NTBT | attributed | validated |
| ICD-11 | LB78.3 | NTBT | index | validated |
| ICD-11 | LB78.Y | NTBT | index | validated |
| UMLS | C0431903 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:498470Non-syndromic complex polydactyly
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:295010OBSOLETE: Central polydactyly of toes referred to · inactive
- ORPHA:295171OBSOLETE: Central polydactyly of fingers, unilateral referred to · inactive
- ORPHA:295173OBSOLETE: Central polydactyly of fingers, bilateral referred to · inactive
- ORPHA:295183OBSOLETE: Central polydactyly of toes, unilateral referred to · inactive
- ORPHA:295185OBSOLETE: Central polydactyly of toes, bilateral referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295004
- This record as JSON: /data/d/295004.json