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: lice infestation (MONDO:0003472)
..Starting node ..Pediculus humanus capitis infestation ()
Child Nodes:
Sister Nodes:
..Pediculus humanus capitis infestation ()
..Pediculus humanus corporis infestation ()
..Pthirus pubis infestation ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3471
Name:	Pediculus humanus capitis infestation
Definition:	A infectious disease involving Pediculus humanus capitis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	head louse infestation; infections, Pediculus humanus capitis; pediculosis capitis; Pediculus capitis; Pediculus capitis [head louse]; Pediculus capitis infestation; Pediculus humanus capitis infection
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal