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, UMDF: 1= Disease, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, Myopathy, SANDO

Disease Browser
Parent Node: Myiasis (D009198)
..Starting node ..Hypodermyiasis (D007000)
Child Nodes:
Sister Nodes:
..Furunculous myiasis (C538194)
..Hypodermyiasis (D007000)
..Screw Worm Infection (D012610)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6035
Name:	Hypodermyiasis
Definition:	Infestation with larvae of the genus Hypoderma, the warble fly.
Alternative IDs:	DO:DOID:12926
ParentIDs:	MESH:D009198
TreeNumbers:	C03.858.211.503.398
Synonyms:	Hypodermyiases
Slim Mappings:	Parasitic disease
Reference:	MedGen: D007000 MeSH: D007000 OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal