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: candidiasis (MONDO:0002026)
Parent Node: digestive system infectious disease (MONDO:0043424)
Parent Node: mouth disease (MONDO:0006858)
..Starting node ..oral candidiasis ()
Child Nodes:
Sister Nodes:
..adenoid hypertrophy ()
..alveolar periostitis ()
..burning mouth syndrome ()
..commissural lip fistula ()
..lichen planus, oral ()
..lip disease ()
..Ludwig's angina ()
..maxillary sinus cholesteatoma ()
..maxillary sinusitis ()
..mouth mucosa disease ()
..neoplasm of floor of mouth ()
..neoplasm of jaw ()
..odontoma ()
..oral candidiasis ()
..oral cavity neoplasm ()
..oral Crohn disease ()
..oral hairy leukoplakia ()
..oral leukoedema ()
..oral submucous fibrosis ()
..oral tuberculosis ()
..salivary gland disease ()
..tongue disease ()
..tooth disease ()
..uvulitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5886
Name:	oral candidiasis
Definition:	Infection of the mucosal lining of the mouth with the fungus Candida albicans.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	candidiasis of mouth; mouth candidiasis; oral moniliasis; thrush; thrush, oral
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: ATP8B1;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal