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: herpes simplex infectious disease (MONDO:0004609)
Parent Node: skin infection (MONDO:0021201)
..Starting node ..herpes simplex dermatitis ()
Child Nodes:
Sister Nodes:
..cercarial dermatitis ()
..cutaneous diphtheria ()
..deep seated dermatophytosis ()
..Demodex folliculitis ()
..dermatophytosis ()
..erysipelas ()
..gonococcal keratitis ()
..herpes simplex dermatitis ()
..herpes zoster dermatitis ()
..impetigo ()
..infection by Trypanosoma gambiense ()
..Pthirus pubis infestation ()
..scabies ()
..tinea favosa ()
..tinea infection ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4712
Name:	herpes simplex dermatitis
Definition:	Localized rash characterized by grouped vesicles or pustules on an erythematous base that is caused by herpes simplex virus infection.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	eczema herpeticum; eczema herpeticum (disorder) [ambiguous]; Herpes simplex dermatitis; herpes simplex dermatitis; Herpes simplex dermatitis of eyelid; Herpes simplex eyelid dermatitis; Herpes simplex virus dermatitis; herpes simplex virus eyelid dermatitis; Simplexvirus caused dermatitis; Simplexvi
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal