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: Anaplasmataceae infectious disease (MONDO:0006922)
Parent Node: primary bacterial infectious disease (MONDO:0000314)
Parent Node: tick-borne infectious disease (MONDO:0025294)
..Starting node ..ehrlichiosis ()
Child Nodes:
........heartwater disease ()
........human granulocytic ehrlichiosis ()
........human monocytic ehrlichiosis ()
........sennetsu fever ()
Sister Nodes:
..African swine fever ()
..anaplasmosis ()
..ehrlichiosis ()
..louping ill ()
..Lyme disease ()
..Nairobi sheep disease ()
..Omsk hemorrhagic fever ()
..Powassan encephalitis ()
..Queensland tick typhus ()
..Rickettsia helvetica spotted fever ()
..tick-borne encephalitis ()
..tick-borne relapsing fever ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	16003
Name:	ehrlichiosis
Definition:	Human ehrlichiosis and anaplasmosis describe a group of acute febrile tick-borne diseases characterized by an overlapping clinical picture that includes fever, headache, myalgias, arthralgias, skin eruptions, gastrointestinal symptoms and neurological manifestations. Diseases in this group include human monocytotropic ehrlichiosis (HME), human granulocytotropic anaplasmosis (HGA), and human ehrlichiosis ewingii (HEE) (see these terms).
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	human ehrlichiosis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal