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 ..Majocchi granuloma ()
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:	20709
Name:	Majocchi granuloma
Definition:	An inflammatory and granulomatous, dermatophytic infection that is classified into two forms, depending on the affected individualbs health situation and clinical picture. The first form is mainly observed in healthy individuals and is defined as a perifollicular, papular form induced by penetrating trauma that is mostly observed in the lower extremities. The second form is granulomatous, related to immunosuppression, seen in a nodular form, and usually appears on the upper extremities.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Majocchi's granuloma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal