ORPHA:295193
Zygodactyly type 4
Synonyms: SD1, Castilla type · SD1d · Syndactyly type 1, Castilla type · Syndactyly type 1d · Zygodactyly, Castilla 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 4 | SD1, Castilla type · SD1d · Syndactyly type 1, Castilla type · Syndactyly type 1d · Zygodactyly, Castilla type |
| fr | Zygodactylie type 4 | SD1 type Castilla · SD1d · Syndactylie type 1 type Castilla · Syndactylie type 1d · Zygodactylie type Castilla |
| de | Zygodaktylie Typ 4 | SD1 Typ Castilla · SD1d · Syndaktylie Typ 1d · Syndaktylie Typ 1d, Typ Castilla · Zygodaktylie Typ Castilla |
| es | Zigodactilia tipo 4 | SD1 tipo Castilla · SD1d · Sindactilia tipo 1, tipo Castilla · Sindactilia tipo 1d · Zigodactilia tipo Castilla |
| it | Zigodattilia, tipo 4 | SD1, tipo Castilla · SD1d · Sindattilia tipo 1, tipo Castilla · Sindattilia, tipo 1d · Zigodattilia, tipo Castilla |
| nl | Zygodactylie type 4 | Syndactylie type 1, Castilla-type · Syndactylie type 1d · Zygodactylie, Castilla-type · SD1, Castilla-type · SD1d |
| pt | Zigodactilia tipo 4 | SD1, tipo Castilla · SD1d · Sindactilia tipo 1, tipo Castilla · Sindactilia tipo 1d · Zigodactilia, tipo Castilla |
| pl | Zygodaktylia typu 4 | SD1, typ Castilla · SD1d · Syndaktylia typu 1, typ Castilla · Syndaktylia typu 1d · Zygodaktylia, typ Castilla |
| cs | Zygodaktylie, typ 4 | SD1d · Syndaktylie typ 1d · SD1, Castillův typ · Syndaktylie typ 1, Castillův typ · Zygodaktylie, Castillův typ |
| uk | Зигодактилія, тип 4 | SD1, тип Кастилія · SD1d · Синдактилія типу 1, кастильський тип · Синдактилія типу 1d · Зигодактилія, кастильський тип |
| zh | 并指4型 | 并指（趾）Castilla型 |
| tr | Zigodaktili tip 4 | SD1d · SD1, Castilla tipi · Sindaktili tip 1d · Zigodaktili, Kastilla tipi · Sindaktili tip 1, Kastilla tipi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q70.3 | NTBT | attributed | validated |
| ICD-11 | LB79.Y | NTBT | index | validated |
| MONDO | 0017545 | E | validated | |
| UMLS | C5679981 | 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/295193
- This record as JSON: /data/d/295193.json