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: primary bacterial infectious disease (MONDO:0000314)
Parent Node: staphylococcal infection (MONDO:0024313)
..Starting node ..staphyloenterotoxemia ()
Child Nodes:
Sister Nodes:
..staphylococcal pneumonia ()
..staphylococcal toxemia ()
..staphylococcus aureus infection ()
..staphyloenterotoxemia ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5971
Name:	staphyloenterotoxemia
Definition:	Food poisoning that is caused by Staphylococcal infection.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	staphylococcal food poisoning; staphylococcal toxaemia due to food; staphyloenterotoxicosis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal