ORPHA:90058
Spinal cord injury
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spinal cord injury | |
| fr | Lésion de la moelle épinière | |
| de | Rückenmarkverletzung | |
| es | Daño de la médula espinal | |
| it | Lesione del midollo spinale | |
| nl | Ruggenmergletsel | |
| pt | Lesão traumática da medula espinhal | |
| pl | Uraz rdzenia kręgowego | |
| cs | Poranění míchy | |
| uk | Травма спинного мозку | |
| zh | 脊髓损伤 | |
| tr | Omurilik yaralanması |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | T09.3 | NTBT | attributed | validated |
| ICD-11 | ND51.2 | E | specific | validated |
| MONDO | 0043797 | E | validated | |
| MeSH | D013119 | E | validated | |
| UMLS | C0037929 | E | validated | |
| MedDRA | 10041552 | 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:102000Medullar disease
rare neurological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-5 / 10 000 | 32 / 100 000 | Europe | Value and class | Validated | European Medicines Agency[OTHER] |
| Annual incidence | 1-9 / 100 000 | 3.57 / 100 000 | Canada | Value and class | Validated | 22337075[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
15 annotations · validated 2023-10-05| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0100561 | Spinal cord lesion | |
| Frequent (79-30%) | ||
| HP:0012332 | Abnormal autonomic nervous system physiology | |
| HP:0002315 | Headache | |
| HP:0003474 | Somatic sensory dysfunction | |
| HP:0001257 | Spasticity | |
| HP:0002839 | Urinary bladder sphincter dysfunction | |
| HP:0010549 | Weakness due to upper motor neuron dysfunction | |
| Occasional (29-5%) | ||
| HP:0012533 | Allodynia | |
| HP:0012534 | Dysesthesia | |
| HP:0003072 | Hypercalcemia | |
| HP:0007185 | Loss of consciousness | |
| HP:0002590 | Paralytic ileus | |
| HP:0003396 | Syringomyelia | |
| HP:0000016 | Urinary retention | |
| HP:0002953 | Vertebral compression fracture | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 28161028[PMID]_32859390[PMID]_37761417[PMID]_28161027[PMID]
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/90058
- This record as JSON: /data/d/90058.json