MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: skin infection (MONDO:0021201)
Parent Node: superficial mycosis (MONDO:0024268)
..Starting node ..dermatophytosis ()
Child Nodes:
........dermatophytosis of groin and perianal area ()
........dermatophytosis of scalp or beard ()
........ectothrix infectious disease ()
........endothrix infectious disease ()
........Majocchi granuloma ()
........tinea barbae ()
........tinea corporis ()
........tinea manuum ()
........tinea pedis ()
........tinea profunda ()
........tinea unguium ()
Sister Nodes:
..dermatophytosis ()
..piedra ()
..pityriasis versicolor ()
..tinea nigra ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4678
Name:	dermatophytosis
Definition:	A common fungal infection of the stratum corneum of the skin, hair, or nails by a dermatophyte. It is characterized by itching, inflammation, redness of the skin, small papular vesicles, central clearing, fissures, scaling, and/or hair loss in the affected area.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	dermatomycosis; fungal skin disease; fungal skin diseases; ringworm; skin disease, fungal; skin diseases, fungal
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal