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: digestive system neoplasm (MONDO:0021223)
Parent Node: head and neck neoplasm (MONDO:0005586)
Parent Node: tongue disease (MONDO:0001165)
..Starting node ..tongue neoplasm ()
Child Nodes:
........benign neoplasm of tongue ()
........tongue cancer ()
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:	21240
Name:	tongue neoplasm
Definition:	A neoplasm (disease) that involves the tongue.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	neoplasm of the tongue; neoplasm of tongue; tongue neoplasm (disease); tongue tumor; tumor of the tongue; tumor of tongue
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal