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Descriptor English: Dentinogenesis Imperfecta
Descriptor Spanish: Dentinogénesis Imperfecta
Descriptor dentinogénesis imperfecta
Entry term(s) dentina opalescente
dentina opalescente hereditaria
dentinogénesis imperfecta 1
dentinogénesis imperfecta sin osteogénesis imperfecta
dentinogénesis imperfecta tipo 2 de Shields
dentinogénesis imperfecta tipo II de Shields
dientes de Capdepont
dientes opalescentes sin osteogénesis imperfecta
Scope note: Trastorno autosómico dominante del desarrollo del diente, caracterizado por la presencia de una dentina opalescente que produce alteraciones del color de los dientes, de azul oscuro a marrón. La dentina se forma mal, con un contenido mineral anormalmente bajo. El canal de la pulpa está obliterado, pero el esmalte es normal. Los dientes suelen desgastarse con rapidez, dejando muñones cortos y marrones. (Dorland, 27th ed)
Descriptor Portuguese: Dentinogênese Imperfeita
Descriptor French: Dentinogenèse imparfaite
Entry term(s): Capdepont Teeth
Dentin, Opalescent
Dentinogenesis Imperfecta 1
Dentinogenesis Imperfecta without Osteogenesis Imperfecta
Dentinogenesis Imperfecta, Shields Type 2
Dentinogenesis Imperfecta, Shields Type II
Hereditary Opalescent Dentin
Imperfecta 1, Dentinogenesis
Imperfecta, Dentinogenesis
Opalescent Dentin
Opalescent Dentin, Hereditary
Opalescent Teeth without Osteogenesis Imperfecta
Teeth, Capdepont
Tree number(s): C07.650.800.270
C07.793.700.270
C16.131.850.800.270
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D003811
Scope note: An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 65
History Note: 65
Related: Osteogenesis Imperfecta MeSH
DeCS ID: 3826
Unique ID: D003811
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2016/02/08
Dentinogenesis Imperfecta - Preferred
Concept UI M0005958
Scope note An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.
Preferred term Dentinogenesis Imperfecta
Entry term(s) Imperfecta, Dentinogenesis
Opalescent Dentin - Narrower
Concept UI M0525156
Preferred term Opalescent Dentin
Entry term(s) Capdepont Teeth
Dentin, Opalescent
Imperfecta 1, Dentinogenesis
Teeth, Capdepont
Dentinogenesis Imperfecta without Osteogenesis Imperfecta - Narrower
Concept UI M0551534
Preferred term Dentinogenesis Imperfecta without Osteogenesis Imperfecta
Entry term(s) Dentinogenesis Imperfecta, Shields Type 2
Dentinogenesis Imperfecta, Shields Type II
Opalescent Teeth without Osteogenesis Imperfecta
Hereditary Opalescent Dentin - Narrower
Concept UI M0005959
Preferred term Hereditary Opalescent Dentin
Entry term(s) Opalescent Dentin, Hereditary
Dentinogenesis Imperfecta 1 - Narrower
Concept UI M000738554
Preferred term Dentinogenesis Imperfecta 1



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