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 ..mite infestation ()
Child Nodes:
........scabies ()
........trombiculiasis ()
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:	4389
Name:	mite infestation
Definition:	Infestations with arthropods of the subclass acari, superorder Acariformes.
Alternative IDs:
ParentIDs:
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Synonyms:
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal