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: eyelid disease (MONDO:0003382)
Parent Node: herpes zoster dermatitis (MONDO:0021033)
Parent Node: viral eye infection (MONDO:0020950)
..Starting node ..herpes zoster with dermatitis of eyelid ()
Child Nodes:
Sister Nodes:
..cytomegalovirus retinitis ()
..herpes simplex virus keratitis ()
..herpes zoster with dermatitis of eyelid ()
..viral conjunctivitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21032
Name:	herpes zoster with dermatitis of eyelid
Definition:	A form of herpes zoster infection characterized by dermatitis of the skin of the eyelid due to reactivation of latent virus associated with the ophthalmic branch of the trigeminal nerve.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Herpes Zoster Dermatitis of Eyelid; herpes zoster dermatitis of eyelid; Herpes zoster dermatitis of eyelids; herpes zoster dermatitis of eyelids; Herpes zoster with dermatitis of eyelid; herpes zoster with dermatitis of eyelid
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal