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: tongue disease (MONDO:0001165)
..Starting node ..hairy tongue ()
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:	6777
Name:	hairy tongue
Definition:	A benign condition affecting the dorsum of the tongue. It is characterized by defective desquamation resulting in elongation of the filiform papillae. The dorsum of the tongue has a furry appearance and is usually stained black.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	hairy tongue; hairy Tongues; overgrowth of filiform papillae; Tongues, hairy
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal