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: helminthiasis (MONDO:0004664)
..Starting node ..Cestode infectious disease ()
Child Nodes:
........diphyllobothriasis ()
........echinococcosis ()
........mesocestoidiasis ()
........sparganosis ()
........taeniasis ()
Sister Nodes:
..acanthocephaliasis ()
..angiostrongyliasis ()
..Cestode infectious disease ()
..clonorchiasis ()
..dicrocoeliasis ()
..echinostomiasis ()
..fascioliasis ()
..fascioloidiasis ()
..fasciolopsiasis ()
..filariasis ()
..gnathomiasis ()
..helminthiasis, animal ()
..heterophyiasis ()
..hymenolepiasis ()
..intestinal helminthiasis ()
..metagonimiasis ()
..monieziasis ()
..necatoriasis ()
..Nematoda infectious disease ()
..opisthorchiasis ()
..paragonimiasis ()
..schistosomiasis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	42488
Name:	Cestode infectious disease
Definition:	Infections with true tapeworms of the helminth subclass Cestoda.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Bertielliases; Bertielliasis; Cenuriases; Cenuriasis; Cestoda caused disease or disorder; Cestoda disease or disorder; Cestoda infectious disease; cestode infection; cestode infestation; Cestodiasis; Cestodosis; Coenuriases; Coenuriasis; Dipylidiases; Dipylidiasis; disease due to Cestoda; infection,
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal