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: Dermatitis (D003872)
Parent Node: Scalp Dermatoses (D012536)
..Starting node ..Dandruff (D063807)
Child Nodes:
Sister Nodes:
..Adams Oliver syndrome (C538225)
..Akesson syndrome (C535610)
..Cutis Gyrata Syndrome of Beare And Stevenson (C565129)
..Cutis Verticis Gyrata and Mental Deficiency (C565661)
..Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness (C565306)
..Dandruff (D063807)
..Perifolliculitis Capitis Abscedens Et Suffodiens, Familial (C562486)
..Rosenthal-Kloepfer syndrome (C535654)
..Tinea Capitis (D014006) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2963
Name:	Dandruff
Definition:	Excessive shedding of dry scaly material from the scalp in humans.
Alternative IDs:
ParentIDs:	MESH:D003872\|MESH:D012536
TreeNumbers:	C17.800.174.146 \|C17.800.738.353
Synonyms:	Scurf
Slim Mappings:	Skin disease
Reference:	MedGen: D063807 MeSH: D063807 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants