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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 ..Connective Tissue Nevus (C562737)
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:	2677
Name:	Connective Tissue Nevus
Definition:
Alternative IDs:
ParentIDs:	MESH:D009506
TreeNumbers:	C04.557.665.560/C562737
Synonyms:
Slim Mappings:	Cancer
Reference:	MedGen: C562737 MeSH: C562737 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants