ORPHA:717585
Kasabach-Merritt-like phenomenon
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Kasabach-Merritt-like phenomenon | |
| fr | Phénomène de type Kasabach-Merritt | |
| de | Kasabach-Merritt-artiges Phänomen | |
| es | Fenómeno similar al de Kasabach-Merritt | |
| it | Fenomeno simil-Kasabach-Merritt | |
| nl | Kasabach-Merritt-achtig fenomeen | |
| pt | Kasabach-Merritt-like phenomenon | |
| pl | Zjawisko podobne do Kasabacha-Merritta | |
| cs | Kasabach-Merritt-like phenomenon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P54.8 | NTBT | attributed | validated |
| ICD-11 | KA8Y | NTBT | attributed | 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 (2):
- ORPHA:717582Coagulation abnormality associated with a vascular anomaly
rare developmental anomalies during embryogenesis; rare circulatory system diseases - ORPHA:248308Rare hemorrhagic disorder
rare hematological 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/717585
- This record as JSON: /data/d/717585.json