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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: Angioedema (D000799)
..Starting node ..Acquired angioedema (C538173)
Child Nodes:
Sister Nodes:
..Acquired angioedema (C538173)
..Angioedemas, Hereditary (D054179) 2
..Vibratory angioedema (C536347)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	167
Name:	Acquired angioedema
Definition:
Alternative IDs:
ParentIDs:	MESH:D000799
TreeNumbers:	C14.907.079/C538173 \|C17.800.862.945.066/C538173 \|C20.543.480.904.066/C538173
Synonyms:
Slim Mappings:	Cardiovascular disease\|Immune system disease\|Skin disease
Reference:	MedGen: C538173 MeSH: C538173 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants