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: Scalp Dermatoses (D012536)
Parent Node: Tinea (D014005)
..Starting node ..Tinea Capitis (D014006)
Child Nodes:
........Tinea Favosa (D014007)
Sister Nodes:
..Onychomycosis (D014009)
..Tinea Capitis (D014006) 1
..Tinea Pedis (D014008)
..Trichophyton infection (C569516)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11104
Name:	Tinea Capitis
Definition:	Ringworm of the scalp and associated hair mainly caused by species of MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON, which may occasionally involve the eyebrows and eyelashes.
Alternative IDs:
ParentIDs:	MESH:D012536\|MESH:D014005
TreeNumbers:	C01.539.800.200.720.730 \|C01.703.295.872.541 \|C17.800.738.708 \|C17.800.838.208.883.558
Synonyms:	Barbae, Trichophytia Profunda \|Capitides, Trichophytia Profunda \|Capitis Profundas, Tinea \|Capitis Profunda, Tinea \|Capitis, Trichophytia Profunda \|Kerion Celsi \|Profunda Barbae, Trichophytia \|Profunda Capitides, Trichophytia \|Profunda Capitis, Trichophytia \|Prof
Slim Mappings:	Bacterial infection or mycosis\|Skin disease
Reference:	MedGen: D014006 MeSH: D014006 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants