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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: Nevus (D009506)
..Starting node ..Epidermal Nevus (C580062)
Child Nodes:
Sister Nodes:
..Becker Nevus Syndrome (C565735)
..Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
..Connective Tissue Nevus (C562737)
..Dysplastic Nevus Syndrome (D004416)
..Epidermal Nevus (C580062)
..Nevus, Halo (D055882)
..Nevus, Intradermal (D018330)
..Nevus, Pigmented (D009508) 11
..Nevus, Sebaceous of Jadassohn (D054000) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3813
Name:	Epidermal Nevus
Definition:
Alternative IDs:
ParentIDs:	MESH:D009506
TreeNumbers:	C04.557.665.560/C580062
Synonyms:	Epidermal Naevus
Slim Mappings:	Cancer
Reference:	MedGen: C580062 MeSH: C580062 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants