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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: Hypersensitivity, Immediate (D006969)
Parent Node: Skin Diseases, Vascular (D017445)
..Starting node ..Urticaria (D014581)
Child Nodes:
........Angioedema (D000799) 5
........FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 (OMIM:120100)
........Familial dermographism (C536612)
........MUCKLE-WELLS SYNDROME (OMIM:191900)
........Papular urticaria (C537169)
........Urticaria, Aquagenic (C562481)
........Urticaria, Familial Localized Heat (C566011)
Sister Nodes:
..Angioma serpiginosum, autosomal dominant (C536365)
..Angioma serpiginosum, X-linked (C536366)
..Angiomatosis, Bacillary (D016917)
..Behcet Syndrome (D001528)
..Cutis marmorata telangiectatica congenita (C536226)
..Gardner-Diamond syndrome (C535645)
..Giant Cell Arteritis (D013700) 1
..Livedo Reticularis (D054068) 1
..Malignant Atrophic Papulosis (D054853)
..Megalencephaly cutis marmorata telangiectatica congenita (C536142)
..Mucocutaneous Lymph Node Syndrome (D009080) 1
..Polyarteritis Nodosa (D010488) 1
..Pyoderma Gangrenosum (D017511) 1
..Sneddon Syndrome (D018860)
..Takayasu Arteritis (D013625)
..Urticaria (D014581) 12
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11438
Name:	Urticaria
Definition:	A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress.
Alternative IDs:
ParentIDs:	MESH:D006969\|MESH:D017445
TreeNumbers:	C17.800.862.945 \|C20.543.480.904
Synonyms:	Hives \|Urticarias
Slim Mappings:	Immune system disease\|Skin disease
Reference:	MedGen: D014581 MeSH: D014581 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants