Solitary fibrous tumor
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 3 |
| OrphanetNr: | 2126 |
| OMIM Id: |
234820
|
| ICD-10: |
C49.9 |
| UMLs: |
C0018922 |
| MeSH: |
D006393 |
| MedDRA: |
10018825 |
| Snomed: |
134335004 36060005 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal recessive inheritance [Omim] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Soft tissue sarcoma
-Rare oncologic disease |
Symptom Information:
|
|
(HPO:0001626) | Abnormality of the cardiovascular system | 73 / 7739 | ||||
|
|
(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 | ||||
|
|
(OMIM) | Malignant hemangiopericytoma | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|