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 ..ectothrix infectious disease ()
Child Nodes:
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:	243
Name:	ectothrix infectious disease
Definition:	A dermatophyte infection of the hair that infects the hair surface.
Alternative IDs:
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Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal