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: scalp disease (MONDO:0044999)
..Starting node ..dermatophytosis of scalp or beard ()
Child Nodes:
Sister Nodes:
..angiosarcoma of the scalp ()
..dermatophytosis of scalp or beard ()
..psoriasis ()
..seborrheic infantile dermatitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2967
Name:	dermatophytosis of scalp or beard
Definition:	Dermatophytosis involving the stratum corneum of the skin of the scalp and beard area.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	dermatophytosis of scalp; dermatophytosis of scalp; dermatophytosis of scalp and Beard; dermatophytosis of scalp or beard; scalp dermatophytosis; scalp ringworm; tinea capitis; tinea capitis due to Trichophyton rubrum; Trichophyton rubrum tinea capitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal