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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)
Parent Node: Hypersensitivity, Immediate (D006969)
..Starting node ..Vibratory angioedema (C536347)
Child Nodes:
Sister Nodes:
..Anaphylaxis (D000707)
..Asthma, Aspirin-Induced (D055963) 1
..Conjunctivitis, Allergic (D003233)
..Dermatitis, Atopic (D003876) 9
..Eosinophilic Esophagitis (D057765)
..Food Hypersensitivity (D005512) 5
..Ragweed Sensitivity (C566725)
..Respiratory Hypersensitivity (D012130) 30
..Urticaria (D014581) 12
..Vibratory angioedema (C536347)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11604
Name:	Vibratory angioedema
Definition:
Alternative IDs:
ParentIDs:	MESH:D000799\|MESH:D006969
TreeNumbers:	C14.907.079/C536347 \|C17.800.862.945.066/C536347 \|C20.543.480.904.066/C536347 \|C20.543.480/C536347
Synonyms:	Angioedema, vibratory
Slim Mappings:	Cardiovascular disease\|Immune system disease\|Skin disease
Reference:	MedGen: C536347 MeSH: C536347 OMIM: 193050; Genes:
Phenotypes
Disease Causing ClinVar Variants