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: Dental Pulp Diseases (D003788)
..Starting node ..Dental Pulp Calcification (D003784)
Child Nodes:
........DENTIN DYSPLASIA, TYPE II (OMIM:125420)
........Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch (C538148)
Sister Nodes:
..Dental Pulp Calcification (D003784) 2
..Dental Pulp Exposure (D003789)
..Dental Pulp Necrosis (D003790)
..Dentin, Secondary (D003809)
..Pulpitis (D011671)
..Tooth, Nonvital (D019553)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3187
Name:	Dental Pulp Calcification
Definition:
Alternative IDs:
ParentIDs:	MESH:D003788
TreeNumbers:	C07.793.237.252
Synonyms:	Anomalous Dysplasia of Dentin \|Calcification, Dental Pulp \|Calcifications, Dental Pulp \|Coronal Dentin Dysplasia \|Coronal Dentin Dysplasias \|Dental Pulp Calcifications \|Dental Pulp Stone \|Dental Pulp Stones \|Denticle \|Denticles \|Dentin Anomalous Dysplasia \|Dentin A
Slim Mappings:	Mouth disease
Reference:	MedGen: D003784 MeSH: D003784 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants