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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 ..Nevus, Halo (D055882)
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:	8042
Name:	Nevus, Halo
Definition:	A benign skin lesion characterized by a zone of depigmentation surrounding the nevus.
Alternative IDs:
ParentIDs:	MESH:D009506
TreeNumbers:	C04.557.665.560.580
Synonyms:	Halo Nevi \|Halo Nevus \|Leukoderma Acquisitum Centrifugum of Sutton \|Nevi, Halo
Slim Mappings:	Cancer
Reference:	MedGen: D055882 MeSH: D055882 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants