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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: Dermatitis (D003872)
Parent Node: Sebaceous Gland Diseases (D012625)
Parent Node: Skin Diseases, Eczematous (D017443)
Parent Node: Skin Diseases, Papulosquamous (D017444)
..Starting node ..Dermatitis, Seborrheic (D012628)
Child Nodes:
........Copper deficiency, familial benign (C535468)
........Garret Tripp syndrome (C535646)
........Ichthyosis hystrix, Curth Macklin type (C536088)
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:	3235
Name:	Dermatitis, Seborrheic
Definition:	A chronic inflammatory disease of the skin with unknown etiology. It is characterized by moderate ERYTHEMA, dry, moist, or greasy (SEBACEOUS GLAND) scaling and yellow crusted patches on various areas, especially the scalp, that exfoliate as dandruff. Seborrheic dermatitis is common in children and adolescents with HIV INFECTIONS.
Alternative IDs:
ParentIDs:	MESH:D003872\|MESH:D012625\|MESH:D017443\|MESH:D017444
TreeNumbers:	C17.800.174.580 \|C17.800.794.230 \|C17.800.815.580 \|C17.800.859.350
Synonyms:	Dermatitides, Seborrheic \|Dermatitis Seborrheica \|Seborrhea \|Seborrheic Dermatitides \|Seborrheic Dermatitis
Slim Mappings:	Skin disease
Reference:	MedGen: D012628 MeSH: D012628 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants