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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: Hemangiopericytoma (D006393)
Parent Node: Lipoma (D008067)
Parent Node: Rectal Neoplasms (D012004)
..Starting node ..Lipomatous hemangiopericytoma (C537029)
Child Nodes:
Sister Nodes:
..Anus Neoplasms (D001005) 3
..Lipomatous hemangiopericytoma (C537029)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6481
Name:	Lipomatous hemangiopericytoma
Definition:
Alternative IDs:
ParentIDs:	MESH:D006393\|MESH:D008067\|MESH:D012004
TreeNumbers:	C04.557.450.550.400/C537029 \|C04.557.645.380/C537029 \|C04.588.274.476.411.307.790/C537029 \|C06.301.371.411.307.790/C537029 \|C06.405.249.411.307.790/C537029 \|C06.405.469.491.307.790/C537029 \|C06.405.469.860.180.500/C537029
Synonyms:
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: C537029 MeSH: C537029 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants