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: staphylococcal infection (MONDO:0024313)
..Starting node ..staphylococcus aureus infection ()
Child Nodes:
........impetigo ()
........methicillin-resistant staphylococcus aureus infectious disease ()
........Ritter disease ()
........staphylococcus aureus pneumonia ()
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:	5545
Name:	staphylococcus aureus infection
Definition:	infection by Staphylococcus.
Alternative IDs:
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Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal