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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Brain Neoplasms (D001932)
Parent Node: Sarcoma (D012509)
..Starting node ..Cerebral sarcoma (C537946)
Child Nodes:
Sister Nodes:
..Adenosarcoma (D018195) 1
..Carcinosarcoma (D002296) 2
..Cerebral sarcoma (C537946)
..Chondrosarcoma (D002813) 2
..Desmoplastic Small Round Cell Tumor (D058405)
..Endometrial Stromal Tumors (D036821) 1
..Fibrosarcoma (D005354) 2
..Hemangiosarcoma (D006394) 3
..Histiocytoma, Malignant Fibrous (D051677) 1
..Leiomyosarcoma (D007890) 1
..Liposarcoma (D008080) 2
..Lymphangiosarcoma (D008204) 1
..Mixed Tumor, Mesodermal (D018199)
..Myosarcoma (D009217) 6
..Myxosarcoma (D009236)
..Osteosarcoma (D012516) 6
..Phyllodes Tumor (D003557) 1
..Plexosarcoma (C537517)
..Sarcoma, Alveolar Soft Part (D018234)
..Sarcoma, Clear Cell (D018227)
..Sarcoma, Experimental (D012513) 4
..Sarcoma, Kaposi (D012514) 3
..Sarcoma, Myeloid (D023981) 1
..Sarcoma, Small Cell (D018228)
..Sarcoma, Synovial (D013584)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

1953

Name:

Cerebral sarcoma

Definition:

Alternative IDs:

ParentIDs:

MESH:D001932|MESH:D012509

TreeNumbers:

C04.557.450.795/C537946 |C04.588.614.250.195/C537946 |C10.228.140.211/C537946 |C10.551.240.250/C537946

Synonyms:

Familial cerebral sarcomas

Slim Mappings:

Cancer|Nervous system disease

Reference:

MedGen: C537946
MeSH: C537946
OMIM: 117600;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0100244	Fibrosarcoma
3	HP:0002664	Neoplasm

Disease Causing ClinVar Variants