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: enterovirus infectious disease (MONDO:0005747)
Parent Node: skin disease caused by infection (MONDO:0024294)
..Starting node ..hand, foot and mouth disease ()
Child Nodes:
Sister Nodes:
..chickenpox ()
..common wart ()
..conidiobolomycosis ()
..cutaneous candidiasis ()
..Epstein-Barr virus hepatitis ()
..erythema infectiosum ()
..eumycotic mycetoma ()
..exanthema subitum ()
..hand, foot and mouth disease ()
..hepatitis A ()
..hepatitis B ()
..hepatitis C ()
..hepatitis E ()
..herpes zoster ()
..herpetic whitlow ()
..infective dermatitis associated with HTLV-1 ()
..otomycosis ()
..parasitic skin disease ()
..pityriasis versicolor ()
..plantar wart ()
..skin disease caused by bacterial infection ()
..skin infection ()
..variola major infectious disease ()
..virus-associated trichodysplasia spinulosa ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5779
Name:	hand, foot and mouth disease
Definition:	A clinical syndrome that is usually caused by enterovirus infection, and that is characterized by fever, anorexia, and painful sores in the mouth, distal extremities, and/or other sites, including the buttocks.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	hand foot and mouth disease; hand, foot, and mouth disease; HFMD; vesicular stomatitis and exanthem
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal