ORPHA:295012
Syndactyly type 6
Synonyms: Mitten hand · Syndactyly, mitten type · Unilateral syndactyly of digits 2-5
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare non-syndromic syndactyly characterized by unilateral fusion of 2nd to 5th fingers, amalgamation of distal phalanges in a knot-like structure, and fusion of the 2nd and 3rd toe. Some individuals present only with webbing between the 2nd and 3rd toes, without involvement of fingers.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndactyly type 6 | Mitten hand · Syndactyly, mitten type · Unilateral syndactyly of digits 2-5 |
| fr | Syndactylie type 6 | Main en mitaine · Syndactylie type mitaine · Syndactylie unilatérale des doigts 2-5 |
| de | Syndaktylie Typ 6 | Syndaktylie, Typ Mitten · Unilaterale Syndaktylie der Digitalen 2-5 |
| es | Sindactilia tipo 6 | Mano en manopla · Mano en mitón · Sindactilia tipo manopla · Sindactilia tipo mitón · Sindactilia unilateral de los dedos 2-5 |
| it | Sindattilia, tipo 6 | Mano a guantone · Sindattilia unilaterale delle dita II-V · Sindattilia, tipo a guantone |
| nl | Syndactylie type 6 | Syndactylie, want-type · Unilaterale syndactylie van vingers 2-5 · Want-hand |
| pt | Sindactilia tipo 6 | Mão em luva sem dedos ('mitten') · Sindactilia tipo luvas sem dedos ('mitten') · Sindactilia unilateral dos dedos 2-5 |
| pl | Syndaktylia typu 6 | Całkowita syndaktylia (objaw rękawicy) · Jednostronna syndaktylia palców 2-5 · Syndaktylia, typ rękawiczki |
| cs | Jednostranná syndaktylie 2.-5. prstu | Spojená ruka · Syndaktylie, typ mitten · Syndaktylie, typ 6 · Syndaktylie, typ palcové rukavice |
| uk | Синдактилія, тип 6 | Рука в рукавичці · Синдактилія, тип рукавиці · Одностороння синдактилія пальців 2-5 |
| zh | 并指6型 | 2-5指（趾）并指（趾）畸形 |
| tr | Sindaktili tip 6 | Yapışık el · Sindaktili, mitten tip · 2-5 parmakların unilateral sindaktilisi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q70.1 | NTBT | attributed | validated |
| ICD-11 | LB79.Y | NTBT | index | validated |
| MONDO | 0017460 | E | validated | |
| UMLS | C4706525 | 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:90025Non-syndromic syndactyly
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
No children.
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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.
6
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/295012
- This record as JSON: /data/d/295012.json