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: parasitic ectoparasitic infectious disease (MONDO:0002875)
..Starting node ..tungiasis ()
Child Nodes:
Sister Nodes:
..external hirudiniasis ()
..lice infestation ()
..mite infestation ()
..myiasis ()
..tick infestation ()
..tungiasis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	19498
Name:	tungiasis
Definition:	An disease or disorder caused by infection with Tunga penetrans.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	chigger flea; S penetrans; Sarcopsylla penetrans; T penetrans; Tunga penetrans; Tunga penetrans caused disease or disorder; Tunga penetrans disease or disorder; Tunga penetrans infectious disease
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal