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: skin disease caused by bacterial infection (MONDO:0024295)
Parent Node: skin infection (MONDO:0021201)
Parent Node: streptococcal infection (MONDO:0021680)
..Starting node ..erysipelas ()
Child Nodes:
Sister Nodes:
..erysipelas ()
..impetigo ()
..pneumococcal infection ()
..scarlet fever ()
..streptococcal meningitis ()
..streptococcal sore throat ()
..streptococcal toxic-shock syndrome ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1266
Name:	erysipelas
Definition:	an infection of the upper layers of the skin caused by species of streptococcus. Erysipelas results in a fiery red rash with raised edges that can easily be distinguished from the skin around it. The affected skin may be warm to the touch.
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Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal