Disease browser and phenotype portal

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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: Neoplasms by Site (D009371)
Parent Node: Splenic Diseases (D013158)
..Starting node ..Splenic Neoplasms (D013160)
Child Nodes:
........Littoral cell angioma of the spleen (C537031)
Sister Nodes:
..Heterotaxy Syndrome (D059446) 7
..Hypersplenism (D006971) 1
..Splenic Infarction (D013159)
..Splenic Neoplasms (D013160) 1
..Splenic Rupture (D013161) 1
..Tuberculosis, Splenic (D014400)
..Wandering Spleen (D050805)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10539
Name:	Splenic Neoplasms
Definition:	Tumors or cancer of the SPLEEN.
Alternative IDs:
ParentIDs:	MESH:D009371\|MESH:D013158
TreeNumbers:	C04.588.842 \|C15.604.744.680
Synonyms:	Cancer of Spleen \|Cancer of the Spleen \|Cancer, Spleen \|Cancer, Splenic \|Cancers, Spleen \|Cancers, Splenic \|Neoplasm, Spleen \|Neoplasm, Splenic \|Neoplasms, Spleen \|Neoplasms, Splenic \|Spleen Cancer \|Spleen Cancers \|Spleen Neoplasm \|Spleen Neoplasms \|Splenic Cancer \|Spl
Slim Mappings:	Cancer\|Lymphatic disease
Reference:	MedGen: D013160 MeSH: D013160 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants