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: mouth disease (MONDO:0006858)
Parent Node: post-viral disorder (MONDO:0021674)
..Starting node ..oral hairy leukoplakia ()
Child Nodes:
Sister Nodes:
..AIDS dementia complex ()
..AIDS-related disorder ()
..chronic Epstein-Barr virus infection syndrome ()
..hepatitis C induced liver cirrhosis ()
..hepatitis D ()
..herpes zoster ()
..oral hairy leukoplakia ()
..post-infectious neuralgia ()
..rubella encephalitis ()
..simian acquired immunodeficiency syndrome ()
..viral dilated cardiomyopathy ()
..virus associated tumor ()
..Zika virus congenital syndrome ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	743
Name:	oral hairy leukoplakia
Definition:	An epithelial hyperplasia of the oral cavity mucosa associated with Epstein-Barr virus and found almost exclusively in persons with HIV infection. The lesion consists of a white patch that is often corrugated or hairy.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	hairy leukoplakia; hairy leukoplakia of mouth; hairy leukoplakia of oral mucosa; hairy leukoplakia of the mouth; hairy leukoplakia of the oral mucosa; mouth hairy leukoplakia; oral cavity hairy leukoplakia; oral hairy keratosis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal