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: Herpesviridae infectious disease (MONDO:0005794)
..Starting node ..varicella zoster infection ()
Child Nodes:
........chickenpox ()
........congenital varicella syndrome ()
........facial nerve palsy due to herpes zoster infection ()
........herpes zoster ()
........herpes zoster dermatitis ()
........herpetic vulvovaginitis ()
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:	5608
Name:	varicella zoster infection
Definition:	A highly contagious viral infection caused by the varicella zoster virus. Clinically, it may be manifested as shingles or chicken pox.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	varicella zoster infection; Varicella-zoster Virus infection
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: FGF23;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal