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: disorder involving pain (MONDO:0021668)
Parent Node: tongue disease (MONDO:0001165)
..Starting node ..glossodynia ()
Child Nodes:
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:	43237
Name:	glossodynia
Definition:	Painful sensations in the tongue, including a sensation of burning.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	glossalgia; Glossalgias; glossodynia; Glossodynias; Glossopyroses; glossopyrosis; painful tongue; soreness of tongue
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal