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: inflammatory disease (MONDO:0021166)
Parent Node: tongue disease (MONDO:0001165)
..Starting node ..glossitis ()
Child Nodes:
........atrophic glossitis ()
........median rhomboid glossitis ()
Sister Nodes:
..ankyloglossia ()
..digestive duplication cyst of the tongue ()
..fissured tongue ()
..glossitis ()
..glossodynia ()
..hairy tongue ()
..hypertrophy of tongue papillae ()
..tongue neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6771
Name:	glossitis
Definition:	Inflammation of the tongue.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	inflammation of tongue; tongue inflammation
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal