dentinogenesis imperfecta

Preferred Label : dentinogenesis imperfecta;

MeSH definition : 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.;

CISMeF synonym : dentins, hereditary opalescent; dentin, hereditary opalescent; dentinogenesis imperfectas; hereditary opalescent dentins; imperfectas, dentinogenesis; opalescent dentins, hereditary; imperfecta, dentinogenesis;

DeCS synonym : Opalescent Dentin;

MeSH hyponym : dentinogenesis imperfecta without osteogenesis imperfecta; hereditary opalescent dentin; Dentin, Opalescent; Dentinogenesis Imperfecta 1; Imperfecta 1, Dentinogenesis; Capdepont Teeth; Teeth, Capdepont; Dentinogenesis Imperfecta, Shields Type II; Opalescent Teeth without Osteogenesis Imperfecta; Dentinogenesis Imperfecta, Shields Type 2; Opalescent Dentin, Hereditary;

MeSH annotation : a dentin abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Dentinogenesis imperfecta;

Details

Origin ID

D003811;

UMLS CUI

C0011436;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Dentinogenesis imperfecta - Shield's type I (disorder) [SNOMED CT concept]
- Dentinogenesis imperfecta - Shield's type II (disorder) [SNOMED CT concept]
- Dentinogenesis imperfecta 1 [OMIM Phenotype]
- Dentinogenesis imperfecta type 2 [ORDO Disease]
- Dentinogenesis imperfecta, osteogenesis imperfecta [ACR pathology]
- Hereditary disturbances in tooth structure, not elsewhere classified [ICD-10 Sub-category]
- Hereditary disturbances in tooth structure, not elsewhere classified [ICD-10 Sub-category (who)]
- Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (disorder) [SNOMED CT concept]
- Stainton's syndrome [MedDRA LLT]
Currated CISMeF NLP mapping
- Dentinogenesis Imperfecta [NCIt concept]
- Dentinogenesis imperfecta [ICD-11 Subcategory]
- Dentinogenesis imperfecta [HPO term]
- Dentinogenesis imperfecta [MedDRA Preferred Term]
- Dentinogenesis imperfecta [MedDRA LLT]
- Dentinogenesis imperfecta [ORDO Disease]
- Dentinogenesis imperfecta (disorder) [SNOMED CT concept]
- dentinogenesis imperfecta [DO Concept]
- dentinogenesis imperfecta [Disease (Nov.)]
- dentinogenesis imperfecta [SNOMED Notion]
DO Cross reference
- dentinogenesis imperfecta [DO Concept]
HPO term
- Dentinogenesis imperfecta [HPO term]
Manual BTNT mappings - CISMeF
- Dentinogenesis imperfecta type 3 [ORDO Disease]
- Rare disease with dentinogenesis imperfecta [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Hereditary dentin defect [ORDO Disease]
ORDO relation(s)
- Dentinogenesis imperfecta [ORDO Disease]
Record concept(s)
- Dentinogenesis Imperfecta 1 [MeSH concept]
- dentinogenesis imperfecta [MeSH concept]
- dentinogenesis imperfecta without osteogenesis imperfecta [MeSH concept]
- hereditary opalescent dentin [MeSH concept]
- opalescent dentin [MeSH concept]
Related MeSH Supplementary Concept(s)
- cortical defects, wormian bones, and dentinogenesis imperfecta [MeSH Supplementary Concept]
- deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 [MeSH Supplementary Concept]
- dentinogenesis imperfecta, shields type 3 [MeSH Supplementary Concept]
- osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures [MeSH Supplementary Concept]
- osteogenesis imperfecta, type 1A [MeSH Supplementary Concept]
- spondylometaphyseal dysplasia with dentinogenesis imperfecta [MeSH Supplementary Concept]
See also
- osteogenesis imperfecta [MeSH Descriptor]
See also inter- (CISMeF)
- Dentinogenesis imperfecta - Shield's type II (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Dentinogenesis Imperfecta [NCIt concept]
- Dentinogenesis imperfecta [MedDRA Preferred Term]
- Dentinogenesis imperfecta [ORDO Disease]
- Dentinogenesis imperfecta [HPO term]
- Dentinogenesis imperfecta [MedDRA LLT]
- Dentinogenesis imperfecta (disorder) [SNOMED CT concept]
- Rare disease with dentinogenesis imperfecta [ORDO Disease]
- dentinogenesis imperfecta [DO Concept]
- dentinogenesis imperfecta [Disease (Nov.)]
- dentinogenesis imperfecta [SNOMED Notion]
Validated automatic mappings to BTNT
- Dentinogenesis imperfecta type 2 [ORDO Disease]

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