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: burkholderia infectious disease (MONDO:0043953)
Parent Node: primary bacterial infectious disease (MONDO:0000314)
..Starting node ..melioidosis ()
Child Nodes:
Sister Nodes:
..anthrax infection ()
..bartonellosis ()
..botulism ()
..brucellosis ()
..Buruli ulcer disease ()
..campylobacteriosis ()
..chancroid ()
..cholera ()
..diphtheria ()
..ehrlichiosis ()
..glanders ()
..gonorrhea ()
..granuloma inguinale ()
..legionellosis ()
..leprosy ()
..leptospirosis ()
..listeriosis ()
..Lyme disease ()
..melioidosis ()
..mycobacterium avium complex disease ()
..ornithosis ()
..paratyphoid fever ()
..pinta disease ()
..plague ()
..Q fever ()
..relapsing fever ()
..rhinoscleroma ()
..salmonellosis ()
..shigellosis ()
..spirillary rat-bite fever ()
..staphyloenterotoxemia ()
..streptobacillary rat-bite fever ()
..syphilis ()
..tetanus ()
..tuberculosis ()
..tularemia ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	17775
Name:	melioidosis
Definition:	An infection that is caused by Burkholderia pseudomallei, which is found in soil and water; symptoms vary widely, but most commonly include fever, cough, pneumonia, arthralgia, myalgia, and skin ulceration.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	acute and fulminating melioidosis; B pseudomallei infection; Burkholderia pseudomallei caused disease or disorder; Burkholderia pseudomallei disease or disorder; Burkholderia pseudomallei infection; Burkholderia pseudomallei infectious disease; Nightcliff gardener's disease; pseudoglanders; subacute
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal