ORPHA:90025
Non-syndromic syndactyly
- Type
- Category
- Group
- Group of disorders
- Status
- active
A group of rare, congenital, non-syndromic distal limb malformation disorders characterized by webbing or fusion of the fingers or toes, involving soft parts only or including bone structure. The morphological anomaly can be unilateral or bilateral, symmetrical or asymmetrical, depending on the specific type.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic syndactyly | |
| fr | Syndactylie non syndromique | |
| de | Syndaktylie, nicht-syndromale | |
| es | Sindactilia no sindrómica | |
| it | Sindattilia non sindromica | |
| nl | Niet-syndromale syndactylie | |
| pt | Sindactilia não-sindromática | |
| pl | Syndaktylia | |
| cs | Syndaktylie | |
| uk | Несиндромальна синдактилія | |
| zh | 非综合征型并指畸形 | |
| tr | Sendromik olmayan sindaktili |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q70 | E | specific | validated |
| ICD-11 | LB79 | E | specific | validated |
| MONDO | 0019530 | E | validated | |
| MONDO | 19530 | E | validated | |
| MeSH | D013576 | E | validated | |
| UMLS | C5681365 | E | validated | |
| MedDRA | 10042778 | 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:93458Non-syndromic polydactyly, syndactyly and/or hyperphalangy
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
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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/90025
- This record as JSON: /data/d/90025.json