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 infection (MONDO:0021201)
Parent Node: varicella zoster infection (MONDO:0005608)
..Starting node ..herpes zoster dermatitis ()
Child Nodes:
........herpes zoster with dermatitis of eyelid ()
Sister Nodes:
..chickenpox ()
..congenital varicella syndrome ()
..facial nerve palsy due to herpes zoster infection ()
..herpes zoster ()
..herpes zoster dermatitis ()
..herpetic vulvovaginitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21033
Name:	herpes zoster dermatitis
Definition:	Painful, localized rash caused by reactivation of latent varicella zoster virus residing in nerve cell bodies, with resulting infection of the skin in the region supplied by the affected nerve.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	herpes zoster dermatitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal