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: dermatophytosis (MONDO:0004678)
..Starting node ..tinea corporis ()
Child Nodes:
........tinea imbricata ()
Sister 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 ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1461
Name:	tinea corporis
Definition:	a dermatophyte disease of the glabrous skin, excluding the scalp, beard, face, hands, feet, and groin.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	dermatophytosis of the body; dermatophytosis of the trunk
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal