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: cholangitis (MONDO:0004789)
..Starting node ..suppurative cholangitis ()
Child Nodes:
Sister Nodes:
..acute cholangitis ()
..ascending cholangitis ()
..cholecystitis ()
..chronic cholangitis ()
..pericholangitis ()
..sclerosing cholangitis (disease) ()
..suppurative cholangitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1928
Name:	suppurative cholangitis
Definition:	Cholangitis that is characterized by pyogenic organisms.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	suppurative cholangitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal