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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: Capillary Leak Syndrome (D019559)
Parent Node: Hypergammaglobulinemia (D006942)
..Starting node ..Capillary leak syndrome with monoclonal gammopathy (C535573)
Child Nodes:
Sister Nodes:
..Capillary leak syndrome with monoclonal gammopathy (C535573)
..Hyperimmunoglobulin G1(A1) Syndrome (C564173)
..Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis (C565427)
..Mevalonate Kinase Deficiency (D054078)
..Monoclonal Gammopathy of Undetermined Significance (D008998) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1624
Name:	Capillary leak syndrome with monoclonal gammopathy
Definition:
Alternative IDs:
ParentIDs:	MESH:D006942\|MESH:D019559
TreeNumbers:	C14.907.218/C535573 \|C15.378.147.542/C535573 \|C20.683.460/C535573 \|C23.888.512/C535573
Synonyms:	Periodic systemic capillary leak syndrome
Slim Mappings:	Blood disease\|Cardiovascular disease\|Immune system disease\|Signs and symptoms
Reference:	MedGen: C535573 MeSH: C535573 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants