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: bartonellosis (MONDO:0005664)
..Starting node ..trench fever ()
Child Nodes:
Sister Nodes:
..bacillary angiomatosis ()
..cat-scratch disease ()
..Oroya fever ()
..trench fever ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5991
Name:	trench fever
Definition:	An intermittent fever characterized by intervals of chills, fever, and splenomegaly each of which may last as long as 40 hours. It is caused by bartonella quintana and transmitted by the human louse.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Bartonella quintana caused disease or disorder; Bartonella quintana disease or disorder; Bartonella quintana infectious disease; bartonellosis due to Bartonella quintana infection; fever, trench; fevers, trench; His-Werner disease; quintan fever; shin bone fever; tibialgic fever; trench fever; trenc
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal