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 Demineralization (D017001)
..Starting node ..Dental Caries (D003731)
Child Nodes:
........Curly hair-acral keratoderma-caries syndrome (C536220)
........Dental Fissures (D003750)
........Flynn Aird syndrome (C537066)
........Root Caries (D017213)
Sister Nodes:
..Dental Caries (D003731) 4
..Odontohypophosphatasia (C564146)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3179
Name:	Dental Caries
Definition:	Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp.
Alternative IDs:
ParentIDs:	MESH:D017001
TreeNumbers:	C07.793.720.210
Synonyms:	Caries, Dental \|Carious Dentin \|Carious Dentins \|Decay, Dental \|Dental Decay \|Dental White Spot \|Dental White Spots \|Dentin, Carious \|Dentins, Carious \|Spots, White \|Spot, White \|White Spot \|White Spot, Dental \|White Spots \|White Spots, Dental
Slim Mappings:	Mouth disease
Reference:	MedGen: D003731 MeSH: D003731 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants