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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: Splenic Diseases (D013158)
..Starting node ..Hypersplenism (D006971)
Child Nodes:
........Splenomegaly Syndrome With Splenic Germinal Center Hypoplasia And Reduced Circulating T-Helper Cells (C566666)
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:	5479
Name:	Hypersplenism
Definition:	Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marrow, and the potential for reversal by splenectomy.
Alternative IDs:
ParentIDs:	MESH:D013158
TreeNumbers:	C15.604.744.293
Synonyms:	Anemia, Splenic \|Anemias, Splenic \|Splenic Anemia \|Splenic Anemias
Slim Mappings:	Lymphatic disease
Reference:	MedGen: D006971 MeSH: D006971 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants