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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 ..Parapsoriasis (D010267)
Child Nodes:
........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:	8624
Name:	Parapsoriasis
Definition:	The term applied to a group of relatively uncommon inflammatory, maculopapular, scaly eruptions of unknown etiology and resistant to conventional treatment. Eruptions are both psoriatic and lichenoid in appearance, but the diseases are distinct from psoriasis, lichen planus, or other recognized dermatoses. Proposed nomenclature divides parapsoriasis into two distinct subgroups, PITYRIASIS LICHENOIDES and parapsoriasis en plaques (small- and large-plaque parapsoriasis).
Alternative IDs:
ParentIDs:	MESH:D017444
TreeNumbers:	C17.800.859.575
Synonyms:	Dermatoses, Digitate \|Dermatosis, Digitate \|Digitate Dermatoses \|Digitate Dermatosis \|Erythroderma, Maculopapular \|Erythrodermas, Maculopapular \|Maculopapular Erythroderma \|Maculopapular Erythrodermas \|Parakeratosis Variegata \|Parapsoriases \|Parapsoriasis en Plaqu
Slim Mappings:	Skin disease
Reference:	MedGen: D010267 MeSH: D010267 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants