Mast cell sarcoma

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 10
OrphanetNr: 66661
OMIM Id:
ICD-10: C96.2
UMLs: C0036221
MeSH: D012515
MedDRA:
Snomed: 118615008
13583002
188660004

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Mastocytosis
 -Rare hematologic disease
 -Rare oncologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0001744) Splenomegaly Frequent [Orphanet] 337 / 7739
2
 (HPO:0002240) Hepatomegaly Frequent [Orphanet] 467 / 7739
3
 (HPO:0004325) Decreased body weight Frequent [Orphanet] 492 / 7739
4
 (HPO:0100495) Mastocytosis Very frequent [Orphanet] 14 / 7739
5
 (HPO:0012145) Abnormality of multiple cell lineages in the bone marrow Frequent [Orphanet] 11 / 7739
6
 (HPO:0100242) Sarcoma Very frequent [Orphanet] 27 / 7739
7
 (HPO:0002716) Lymphadenopathy Frequent [Orphanet] 129 / 7739
8
 (HPO:0100721) Mediastinal lymphadenopathy Frequent [Orphanet] 19 / 7739
9
 (HPO:0001324) Muscle weakness Frequent [Orphanet] 859 / 7739
10
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: