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: skin disease caused by infection (MONDO:0024294)
Parent Node: varicella zoster infection (MONDO:0005608)
Parent Node: vesiculobullous skin disease (MONDO:0006617)
..Starting node ..chickenpox ()
Child Nodes:
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:	5700
Name:	chickenpox
Definition:	A contagious childhood disorder caused by the varicella zoster virus. It is transmitted via respiratory secretions and contact with chickenpox blister contents. It presents with a vesicular skin rash, usually associated with fever, headache, and myalgias. The pruritic fluid-filled vesicles occur 10-21 days after exposure and last for 3-4 days. An additional 3-4 days of malaise follows before the affected individual feels better. An individual is contagious 1-2 days prior to the appearance of the blisters until all blisters are crusted over. Generally, healthy individuals recover without complications.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	chicken pox; chicken pox infection; chickenpox; Varicella; varicella
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: GNRHR;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal