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: Herpesviridae infectious disease (MONDO:0005794)
..Starting node ..herpes simplex infectious disease ()
Child Nodes:
........congenital herpes simplex virus infection ()
........genital herpes ()
........herpes labialis ()
........herpes simplex dermatitis ()
........herpes simplex encephalitis ()
........herpes simplex virus gingivostomatitis ()
........herpes simplex virus keratitis ()
........herpetic whitlow ()
Sister Nodes:
..congenital herpes virus infection ()
..cytomegalovirus infection ()
..Epstein-Barr virus infection ()
..herpes simplex infectious disease ()
..herpetic gastritis ()
..human herpesvirus 8 infection ()
..infectious bovine rhinotracheitis ()
..malignant catarrh ()
..roseolovirus infectious disease ()
..varicella zoster infection ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4609
Name:	herpes simplex infectious disease
Definition:	A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.)
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	herpes simplex; herpes simplex complex; herpes simplex infection; herpes simplex viral infection; Herpesvirus hominis disease; Simplexvirus caused disease or disorder; Simplexvirus disease or disorder; Simplexvirus infectious disease
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal