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)
Parent Node: foot disease (MONDO:0044989)
..Starting node ..tinea pedis ()
Child Nodes:
Sister Nodes:
..ankle injury ()
..double fingernail of fifth finger ()
..Freiberg disease ()
..heel spur ()
..non-syndromic brachydactyly of toes ()
..plantar fibromatosis ()
..plantar verrucous skin carcinoma ()
..plantar wart ()
..tinea pedis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5984
Name:	tinea pedis
Definition:	Dermatological pruritic lesion in the feet, caused by Trichophyton rubrum, T. mentagrophytes, or Epidermophyton floccosum.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	athlete's foot; dermatophytosis of foot; dermatophytosis of pes; pes dermatophytosis; ringworm of foot
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: NPHP1;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal