Disease Browser
Parent Node: Tooth Diseases (D014076) ..Starting node .. Tooth Discoloration (D014075) Child Nodes:
........Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth (C566560) Sister 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) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 11144
Name: Tooth Discoloration
Definition: Any change in the hue, color, or translucency of a tooth due to any cause. Restorative filling materials, drugs (both topical and systemic), pulpal necrosis, or hemorrhage may be responsible. (Jablonski, Dictionary of Dentistry, 1992, p253)
Alternative IDs:
ParentIDs: MESH:D014076
TreeNumbers: C07.793.735
Synonyms: Discolorations, Tooth |Discoloration, Tooth |Tooth Discolorations
Slim Mappings: Mouth disease
Reference:
MedGen: D014075
MeSH: D014075
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants