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: Epstein-Barr virus infection (MONDO:0005111)
Parent Node: skin disease caused by infection (MONDO:0024294)
Parent Node: viral hepatitis (MONDO:0006011)
..Starting node ..Epstein-Barr virus hepatitis ()
Child Nodes:
Sister Nodes:
..Epstein-Barr virus hepatitis ()
..hepatitis A ()
..hepatitis B ()
..hepatitis C ()
..hepatitis E ()
..hepatitis, viral, animal ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	286
Name:	Epstein-Barr virus hepatitis
Definition:	A viral hepatitis that results_in inflammation, located_in liver, has_material_basis_in Human herpesvirus 4 and has_symptom headache, has_symptom fatigue, has_symptom fever, has_symptom abdominal pain, has_symptom nausea, and has_symptom jaundice.
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Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal