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: Bell's palsy (MONDO:0005665)
Parent Node: infectious disease with peripheral neuropathy (MONDO:0016104)
Parent Node: varicella zoster infection (MONDO:0005608)
..Starting node ..facial nerve palsy due to herpes zoster infection ()
Child Nodes:
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:	17606
Name:	facial nerve palsy due to herpes zoster infection
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	facial nerve palsy due to VZV; facial nerve paralysis due to VZV; Hunt syndrome (formerly); Hunt's syndrome (formerly); Ramsay Hunt syndrome; Ramsay Hunt syndrome type 2 (formerly)
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal