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: Hepadnaviridae infectious disease (MONDO:0005786)
Parent Node: skin disease caused by infection (MONDO:0024294)
Parent Node: viral hepatitis (MONDO:0006011)
..Starting node ..hepatitis B ()
Child Nodes:
........chronic hepatitis B ()
........hepatitis D ()
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:	5344
Name:	hepatitis B
Definition:	A viral infection caused by the hepatitis B virus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	chronic hepatitis B; Hepatitis B; Hepatitis B infection; hepatitis B infection; Hepatitis B virus caused hepatitis; Hepatitis B virus hepatitis; hepatitis type B; serum hepatitis; viral Hepatitis B
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal