ORPHA:295189
Zygodactyly type 2
Synonyms: SD1, Lueken type · SD1b · Syndactyly type 1, Lueken type · Syndactyly type 1b · Zygodactyly, Lueken type
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Syndactyly type 1
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Zygodactyly type 2 | SD1, Lueken type · SD1b · Syndactyly type 1, Lueken type · Syndactyly type 1b · Zygodactyly, Lueken type |
| fr | Zygodactylie type 2 | SD1 type Lueken · SD1b · Syndactylie type 1 type Lueken · Syndactylie type 1b · Zygodactylie type Lueken |
| de | Zygodaktylie Typ 2 | SD1, Typ Lueken · SD1b · Syndaktylie Typ 1, Typ Lueken · Syndaktylie Typ 1b · Zygodaktylie Typ Lueken |
| es | Zigodactilia tipo 2 | SD1 tipo Lueken · SD1b · Sindactilia tipo 1, tipo Lueken · Sindactilia tipo 1b · Zigodactilia tipo Lueken |
| it | Zigodattilia, tipo 2 | SD1, tipo Lueken · SD1b · Sindattilia tipo 1, tipo Lueken · Sindattilia, tipo 1b · Zigodattilia, tipo Lueken |
| nl | Zygodactylie type 2 | Zygodactylie, Lueken-type · SD1, Lueken-type · SD1b · Syndactylie type 1, Lueken-type · Syndactylie type 1b |
| pt | Zigodactilia tipo 2 | SD1, tipo Lueken · SD1b · Sindactilia tipo 1, tipo Lueken · Sindactilia tipo 1b · Zigodactilia, tipo Lueken |
| pl | Zygodaktylia typu 2 | SD1, typ Luekena · SD1b · Syndaktylia typu 1, typ Luekena · Syndaktylia typu 1b · Zygodaktylia, typ Luekena |
| cs | Zygodaktylie, typ 2 | SD1b · Syndaktylie, typ 1b · SD1, Leukenův typ · Syndaktylie typ 1, Leukenův typ · Zygodaktylie, Leukenův typ |
| uk | Зигодактилія, тип 2 | SD1, тип Lueken · SD1b · Синдактилія типу 1, тип Люкена · Синдактилія типу 1b · Зигодактилія, тип Люкена |
| zh | 并指2型 | 并指（趾）1型 Lueken型 |
| tr | Zigodaktili tip 2 | SD1b · SD1, Lueken tipi · Sindaktili tip 1b · Zigodaktili, Lueken tipi · Sindaktili tip 1, Lueken tipi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q70.0 | BTNT | attributed | validated |
| ICD-10 | Q70.1 | BTNT | attributed | validated |
| ICD-10 | Q70.3 | BTNT | attributed | validated |
| ICD-11 | LB79.Y | NTBT | index | validated |
| MONDO | 0017543 | E | validated | |
| UMLS | C5679982 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:93402Syndactyly type 1
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295189
- This record as JSON: /data/d/295189.json