Disease browser and phenotype 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

Disease Browser
Parent Node: Stomatognathic Diseases (D009057)
..Starting node ..Tooth Diseases (D014076)
Child Nodes:
........Bork Stender Schmidt syndrome (C536576)
........Bruxism (D002012) 2
........Dental Deposits (D003741) 3
........Dental Leakage (D003763)
........Dental Pulp Diseases (D003788) 8
........Dentin Sensitivity (D003807)
........Failure of Tooth Eruption, Primary (C565114)
........Fluorosis, Dental (D009050)
........Focal Infection, Dental (D005491)
........Hypercementosis (D006936)
........Hypoplasia of Teeth Roots (C564144)
........Malocclusion (D008310) 9
........Mouth, Edentulous (D009066) 2
........Tooth Abnormalities (D014071) 130
........Tooth Ankylosis (D020254) 1
........Tooth Demineralization (D017001) 6
........Tooth Discoloration (D014075) 1
........Tooth Eruption, Ectopic (D014079)
........Tooth Injuries (D018677) 3
........Tooth Loss (D016388)
........Tooth Resorption (D014091) 1
........Tooth Wear (D057085) 3
........Tooth, Impacted (D014095)
........Tooth, Unerupted (D014097)
........Toothache (D014098)
Sister Nodes:
..Jaw Diseases (D007571) 199
..Mouth Diseases (D009059) 291
..Pharyngeal Diseases (D010608) 37
..Stomatognathic System Abnormalities (D018640) 329
..Temporomandibular Joint Disorders (D013705) 2
..Tooth Diseases (D014076) 193
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11145
Name:	Tooth Diseases
Definition:
Alternative IDs:
ParentIDs:	MESH:D009057
TreeNumbers:	C07.793
Synonyms:	Diseases, Tooth \|Disease, Tooth \|Tooth Disease
Slim Mappings:	Mouth disease
Reference:	MedGen: D014076 MeSH: D014076 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants