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: infective vaginitis (MONDO:0023557)
Parent Node: varicella zoster infection (MONDO:0005608)
Parent Node: vulvovaginitis (MONDO:0007019)
..Starting node ..herpetic vulvovaginitis ()
Child Nodes:
Sister Nodes:
..herpetic vulvovaginitis ()
..trichomonal vulvovaginitis ()
..vulvovaginal candidiasis ()
..vulvovaginitis, allergic seminal ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21175
Name:	herpetic vulvovaginitis
Definition:	Infection of the vulva and the vagina caused by herpes simplex virus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Herpetic Vulvovaginitis; Herpetic vulvovaginitis; herpetic vulvovaginitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal