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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, Papulosquamous (D017444)
..Starting node ..Lichenoid Eruptions (D017512)
Child Nodes:
........Lichen Nitidus (D017513)
........Lichen Planus (D008010) 3
........Lichen Sclerosus et Atrophicus (D018459)
........Pityriasis Lichenoides (D017514) 1
Sister Nodes:
..Comedones, Familial Dyskeratotic (C562838)
..Dermatitis, Seborrheic (D012628) 3
..Dermatosis Papulosa Nigra (C562379)
..dowling-degos disease (C562924)
..Granulosis Rubra Nasi (C562483)
..Lichenoid Eruptions (D017512) 8
..Parapsoriasis (D010267) 2
..Pityriasis (D010915) 5
..Psoriasis (D011565) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6421
Name:	Lichenoid Eruptions
Definition:	Conditions in which there is histological damage to the lower epidermis along with a grouped chronic inflammatory infiltrate in the papillary dermis disturbing the interface between the epidermis and dermis. LICHEN PLANUS is the prototype of all lichenoid eruptions. (From Rook et al., Textbook of Dermatology, 4th ed, p398)
Alternative IDs:
ParentIDs:	MESH:D017444
TreeNumbers:	C17.800.859.475
Synonyms:	Eruption, Licheniform \|Eruption, Lichenoid \|Eruptions, Licheniform \|Eruptions, Lichenoid \|Licheniform Eruption \|Licheniform Eruptions \|Lichenoid Eruption
Slim Mappings:	Skin disease
Reference:	MedGen: D017512 MeSH: D017512 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants