MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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 skin disease (MONDO:0024610)
..Starting node ..parasitic ectoparasitic infectious disease ()
Child Nodes:
........external hirudiniasis ()
........lice infestation ()
........mite infestation ()
........myiasis ()
........tick infestation ()
........tungiasis ()
Sister Nodes:
..cercarial dermatitis ()
..cutaneous leishmaniasis ()
..Demodex folliculitis ()
..demodicidosis of sebaceous gland ()
..infection by Trypanosoma gambiense ()
..parasitic ectoparasitic infectious disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2875
Name:	parasitic ectoparasitic infectious disease
Definition:	Infestations by parasites which live on, or burrow into, the surface of their host's epidermis. Most ectoparasites are arthropods.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	ectoparasitic infestation; ectoparasitism; infestation, ectoparasitic; Infestations, ectoparasitic
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: NLRP3;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal