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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: Skin Diseases, Vesiculobullous (D012872)
Parent Node: Urticaria (D014581)
..Starting node ..Papular urticaria (C537169)
Child Nodes:
Sister 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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8587
Name:	Papular urticaria
Definition:
Alternative IDs:
ParentIDs:	MESH:D012872\|MESH:D014581
TreeNumbers:	C17.800.862.945/C537169 \|C17.800.865/C537169 \|C20.543.480.904/C537169
Synonyms:	Bullous papular urticaria - type
Slim Mappings:	Immune system disease\|Skin disease
Reference:	MedGen: C537169 MeSH: C537169 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants