Fibrosarcoma
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 3 |
| OrphanetNr: | 2030 |
| OMIM Id: |
117600
|
| ICD-10: |
|
| UMLs: |
C0016057 |
| MeSH: |
D005354 |
| MedDRA: |
10016632 |
| Snomed: |
53654007 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant inheritance [Omim] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Bone sarcoma
-Rare bone disease -Rare oncologic disease Soft tissue sarcoma -Rare oncologic disease |
Symptom Information:
|
|
(HPO:0100244) | Fibrosarcoma | 6 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
|
|
(OMIM) | Cerebral fibrosarcoma | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|