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: hand disease (MONDO:0044990)
..Starting node ..tinea manuum ()
Child Nodes:
Sister Nodes:
..carpal region disease ()
..double nail for fifth toe ()
..hand dermatosis ()
..non-syndromic brachydactyly of fingers ()
..palmar fibromatosis ()
..tinea manuum ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1699
Name:	tinea manuum
Definition:	A dermatophytosis that involves the hands.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	dermatophytosis of hand; dermatophytosis of manus; manus dermatophytosis; Tinea manus
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal