Disease browser and phenotype 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

Disease Browser
Parent Node: Tooth Diseases (D014076)
..Starting node ..Malocclusion (D008310)
Child Nodes:
........Dental Occlusion, Traumatic (D003769)
........Diastema (D003970) 1
........Malocclusion and Short Stature (C565421)
........Malocclusion, Angle Class I (D008311)
........Malocclusion, Angle Class II (D008312) 1
........Malocclusion, Angle Class III (D008313)
........Open Bite (D024343)
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:	6747
Name:	Malocclusion
Definition:	Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982)
Alternative IDs:
ParentIDs:	MESH:D014076
TreeNumbers:	C07.793.494
Synonyms:	Angle Classification \|Angle's Classification \|Angles Classification \|Bite, Cross \|Bites, Cross \|Classification, Angle's \|Crossbite \|Cross Bite \|Crossbites \|Cross Bites \|Crowdings, Tooth \|Crowding, Tooth \|Malocclusions \|Tooth Crowding
Slim Mappings:	Mouth disease
Reference:	MedGen: D008310 MeSH: D008310 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants