Disease browser and phenotype portal

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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 ..Pityriasis (D010915)
Child Nodes:
........Pityriasis Lichenoides (D017514) 1
........Pityriasis Rosea (D017515)
........Pityriasis Rubra Pilaris (D010916) 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:	8965
Name:	Pityriasis
Definition:	A name originally applied to a group of skin diseases characterized by the formation of fine, branny scales, but now used only with a modifier. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D017444
TreeNumbers:	C17.800.859.600
Synonyms:	Pityriases
Slim Mappings:	Skin disease
Reference:	MedGen: D010915 MeSH: D010915 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants