MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: post-viral disorder (MONDO:0021674)
Parent Node: skin disease caused by infection (MONDO:0024294)
Parent Node: varicella zoster infection (MONDO:0005608)
Parent Node: vesiculobullous skin disease (MONDO:0006617)
..Starting node ..herpes zoster ()
Child Nodes:
........geniculate herpes zoster ()
........ophthalmic herpes zoster ()
........zoster sine herpete ()
Sister Nodes:
..autoimmune bullous skin disease ()
..cellulitis (disease) ()
..chickenpox ()
..eosinophilic pustular folliculitis ()
..epidermolysis bullosa ()
..gas gangrene ()
..herpes zoster ()
..papular urticaria ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5609
Name:	herpes zoster
Definition:	A common dermal and neurologic disorder caused by reactivation of the varicella-zoster virus that has remained dormant within dorsal root ganglia, often for decades, after the patient's initial exposure to the virus in the form of varicella (chickenpox). It is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	herpes zona; herpes Zoster; postherpetic neuralgia; shingles; Zoster
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: DMP1;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal