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: mite infestation (MONDO:0004389)
Parent Node: skin infection (MONDO:0021201)
..Starting node ..scabies ()
Child Nodes:
........Norwegian scabies ()
Sister Nodes:
..cercarial dermatitis ()
..cutaneous diphtheria ()
..deep seated dermatophytosis ()
..Demodex folliculitis ()
..dermatophytosis ()
..erysipelas ()
..gonococcal keratitis ()
..herpes simplex dermatitis ()
..herpes zoster dermatitis ()
..impetigo ()
..infection by Trypanosoma gambiense ()
..Pthirus pubis infestation ()
..scabies ()
..tinea favosa ()
..tinea infection ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4525
Name:	scabies
Definition:	A contagious skin infection that is caused by the burrowing parasitic mite, Sarcoptes scabiei, and is characterized by intense itching and small, raised red spots in the area of the mite burrows.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	infestation by Sarcoptes scabiei; infestation by Sarcoptes scabiei var hominis; Sarcoptes scabiei caused disease or disorder; Sarcoptes scabiei disease or disorder; Sarcoptes scabiei infectious disease; sarcoptic itch
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal