Acquired aneurysmal subarachnoid hemorrhage
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare, life threatening rare neurologic disease characterized by a sudden rupture of an intracranial aneurysm into the subarachnoid space. It usually presents with a sudden, severe, excruciating headache accompanied by nausea, vomiting and syncope. Other features may include focal neurological signs, third and sixth nerve palsies, seizures and cardiac failure. Early complications include rebleeding, hydrocephalus, and seizures.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired aneurysmal subarachnoid hemorrhage | |
| fr | Hémorragie subarachnoïdienne par rupture d'anévrisme intracrânien, forme acquise | |
| de | Aneurysmatische Subarachnoidalblutung, erworbene | |
| es | Hemorragia subaracnoidea aneurismática adquirida | |
| it | Emorragia subaracnoidea aneurismatica acquisita | |
| nl | Verworven aneurysmale subarachnoïdale hemorragie | |
| pt | Hemorragia subaracnóidea aneurismática | |
| pl | Nabyty krwotok podpajęczynówkowy z pkniętego tętniaka | |
| cs | Získané subarachnoideální krvácení z aneuryzmatu | |
| uk | Набутий аневризматичний субарахноїдальний крововилив | |
| zh | 获得性动脉瘤蛛网膜下腔出血 | |
| tr | Edinsel anevrizmal subaraknoid kanama |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | I60.9 | NTBT | inclusion | validated |
| ICD-11 | 8B01.0 | E | specific | validated |
| MONDO | 0019543 | E | validated | |
| UMLS | C0338572 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:71281Rare central nervous system and retinal vascular disease
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-5 / 10 000 | 10 / 100 000 | Europe | Value and class | Validated | European Medicines Agency 2015[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
34 annotations · validated 2020-03-13| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0009145 | Abnormal cerebral artery morphology | |
| Frequent (79-30%) | ||
| HP:0001342 | Cerebral hemorrhage | |
| HP:0100543 | Cognitive impairment | |
| HP:0001259 | Coma | |
| HP:0001133 | Constriction of peripheral visual field | |
| HP:0002315 | Headache | |
| HP:0000822 | Hypertension | |
| HP:0002354 | Memory impairment | |
| HP:0002018 | Nausea | |
| HP:0012250 | ST segment depression | |
| HP:0025637 | Vasospasm | |
| HP:0002013 | Vomiting | |
| Occasional (29-5%) | ||
| HP:0030955 | Alcoholism | |
| HP:0002637 | Cerebral ischemia | |
| HP:0001635 | Congestive heart failure | |
| HP:0006824 | Cranial nerve paralysis | |
| HP:0004302 | Functional motor deficit | |
| HP:0000238 | Hydrocephalus | |
| HP:0003124 | Hypercholesterolemia | |
| HP:0003074 | Hyperglycemia | |
| HP:0031885 | Hyperglycorrhachia | |
| HP:0000821 | Hypothyroidism | |
| HP:0031058 | Impairment of activities of daily living | |
| HP:0002490 | Increased CSF lactate | |
| HP:0001974 | Increased total leukocyte count | |
| HP:0002140 | Ischemic stroke | |
| HP:0001712 | Left ventricular hypertrophy | |
| HP:0001658 | Myocardial infarction | |
| HP:0002344 | Progressive neurologic deterioration | |
| HP:0005184 | Prolonged QTc interval | |
| HP:0001250 | Seizure | |
| HP:0001279 | Syncope | |
| HP:0000505 | Visual impairment | |
| Very rare (<4-1%) | ||
| HP:0040075 | Hypopituitarism | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 30535853[PMID]_24670311[PMID]_29623945[PMID]_27316915[PMID]_31051460[PMID]_30366144[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/90065
- This record as JSON: /data/d/90065.json