Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
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Preferred Name

Dentinogenesis Imperfecta
Synonyms

Opalescent Dentin, Hereditary
Definitions

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.
ID

http://purl.bioontology.org/ontology/MESH/D003811
altLabel

Opalescent Dentin, Hereditary

Dentinogenesis Imperfecta without Osteogenesis Imperfecta

Dentin, Opalescent

Teeth, Capdepont

Hereditary Opalescent Dentin

Dentinogenesis Imperfecta, Shields Type 2

Dentinogenesis Imperfecta 1

Opalescent Teeth without Osteogenesis Imperfecta

Dentinogenesis Imperfecta, Shields Type II

Capdepont Teeth

Opalescent Dentin
AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui

C2973527

C5444410

C4049050

C0011436

C0205730
DC

1
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.
DX

19650101
FX

D010013
HN

65
Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469
Inverse of RO

http://purl.bioontology.org/ontology/MESH/D010013
Machine permutation

65
Mapped from

http://purl.bioontology.org/ontology/MESH/C563487

http://purl.bioontology.org/ontology/MESH/C536041

http://purl.bioontology.org/ontology/MESH/C538216

http://purl.bioontology.org/ontology/MESH/C565316

http://purl.bioontology.org/ontology/MESH/C565734

http://purl.bioontology.org/ontology/MESH/C535792
MDA

19990101
MMR

20210305
MN

C07.793.700.270

C07.650.800.270

C16.131.850.800.270
notation

D003811
prefLabel

Dentinogenesis Imperfecta
TERMUI

T811393

T781516

T000892120

T011349

T000892121

T011350

T811389

T781517

T781518
TH

NLM (2017)

UNK (19XX)

NLM (1966)

NLM (2012)

ORD (2010)

OMIM (2013)

GHR (2014)
tui

T019

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D014071
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http://purl.bioontology.org/ontology/ICD10CM/K00.5 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI
http://purl.obolibrary.org/obo/HP_0000703 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.obolibrary.org/obo/DOID_4154 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_4154 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/125485 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://www.orpha.net/ORDO/Orphanet_49042 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036675 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU036675 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/LA30.8 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.obolibrary.org/obo/MONDO_0018849 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0018849 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/125490 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84667 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM