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 ..myiasis ()
Child Nodes:
........cavitary myiasis ()
........cutaneous myiasis ()
........hypodermyiasis ()
........screw worm infectious disease ()
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:	19147
Name:	myiasis
Definition:	The infection of a fly larva (maggot) in human tissue, which most commonly occurs in tropical climates. Affected tissues most commonly include skin, especially if open wounds are present, nasal passages, ears, and eyes.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	infestation by fly larvae; infestation by maggots; maggot infestation; myiasis, unspecified
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal