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 ..paragonimiasis ()
Child Nodes:
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:	5895
Name:	paragonimiasis
Definition:	A parasitic infection caused by trematodes of the Paragonimus genus. Humans are infected from ingestion of raw or undercooked food. It results in chronic lung infection and eosinophilia.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	infection by Paragonimus; lung fluke disease; lung fluke infection; Paragonimus westermani caused disease or disorder; Paragonimus westermani disease or disorder; Paragonimus westermani infection; Paragonimus westermani infectious disease; pulmonary paragonimiasis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal