ORPHA:295199
Synpolydactyly type 3
Synonyms: SD2, Malik type · SD2c · SPD, Malik type · SPD3 · Synpolydactyly, Malik type
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Syndactyly type 2
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Synpolydactyly type 3 | SD2, Malik type · SD2c · SPD, Malik type · SPD3 · Synpolydactyly, Malik type |
| fr | Sympolydactylie type 3 | SD2 type Malik · SD2c · SPD type Malik · SPD3 · Sympolydactylie type Malik |
| de | Synpolydaktylie Typ 3 | SD2 Typ Malik · SD2c · SPD Typ Malik · SPD3 · Synpolydaktylie, Typ Malik |
| es | Polisindactilia tipo 3 | Polisindactilia tipo Malik · SD2 tipo Malik · SD2c · SPD tipo Malik · SPD3 |
| it | Sinpolidattilia, tipo 3 | SD2, tipo Malik · SD2c · SPD, tipo Malik · SPD3 · Sinpolidattilia, tipo Malik |
| nl | Synpolydactylie type 3 | SD2, Malik-type · SD2c · SPD, Malik-type · SPD3 · Synpolydactylie, Malik-type |
| pt | Simpolidactilia, tipo 3 | SD2, tipo Malik · SD2c · SPD, tipo Malik · SPD3 · Simpolidactilia, tipo Malik |
| pl | Synpolidaktylia typu 3 | SD2, typ Malika · SD2c · SPD, typ Malika · SPD3 · Synpolidaktylia, typ Malika |
| cs | Synpolydaktylie, typ 3 | SD2c · SPD3 · SD2, Malikův typ · SPD, Malikův typ · Synpolydaktylie, Malikův typ |
| uk | Синполідактилія, тип 3 | SD2, тип Малік · SD2c · SPD, тип Малік · SPD3 · Синполідактилія, тип Маліка |
| zh | 联指3型 | 并指（趾）Malik型 |
| tr | Sinpolidaktili tip 3 | SD2c · SPD3 · SD2, Malik tipi · SPD, Malik tipi · Sinpolidaktili, Malik tipi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 610234 | E | validated | |
| ICD-10 | Q70.0 | BTNT | attributed | validated |
| ICD-10 | Q70.2 | BTNT | attributed | validated |
| ICD-11 | LB79.Y | NTBT | index | validated |
| MONDO | 0012447 | E | validated | |
| MeSH | C565216 | E | validated | |
| UMLS | C1853255 | 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:93403Syndactyly type 2
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.
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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/295199
- This record as JSON: /data/d/295199.json