SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Dentinogenesis imperfecta
Synonyms

Hereditary opalescent dentin

Dentinogenesis imperfecta (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/196286005

Active

1

altLabel

Hereditary opalescent dentin

Dentinogenesis imperfecta (disorder)

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

J0051

cui

C0011436

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/49755003

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/84540008

Has pathological process

http://purl.bioontology.org/ontology/SNOMEDCT/308490002

notation

196286005

Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/255399007

prefLabel

Dentinogenesis imperfecta

Subset member

6011000124106~MAPADVICE~IF SKELETAL DYSPLASIA WITH WORMIAN BONE, MULTIPLE FRACTURES, DENTINOGENESIS IMPERFECTA SYNDROME CHOOSE Q78.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~ALWAYS K00.5

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF SKELETAL DYSPLASIA WITH WORMIAN BONE, MULTIPLE FRACTURES, DENTINOGENESIS IMPERFECTA SYNDROME CHOOSE M84.60X? | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | EPISODE OF CARE INFORMATION NEEDED | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF GOLDBLATT SYNDROME CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~F78.A9

6011000124106~MAPADVICE~IF SKELETAL DYSPLASIA WITH WORMIAN BONE, MULTIPLE FRACTURES, DENTINOGENESIS IMPERFECTA SYNDROME CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~4

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPTARGET~Q87.1

6011000124106~MAPRULE~IFA 733468006 | Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome |

6011000124106~MAPADVICE~IF DENTINOGENESIS IMPERFECTA, SHORT STATURE, HEARING LOSS, INTELLECTUAL DISABILITY SYNDROME CHOOSE Q87.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~M84.60X?

6011000124106~MAPRULE~IFA 279309008 | Osteogenesis imperfecta, type IV B |

6011000124106~MAPRULE~IFA 717823001 | Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder) |

6011000124106~MAPADVICE~IF DENTINOGENESIS IMPERFECTA, SHORT STATURE, HEARING LOSS, INTELLECTUAL DISABILITY SYNDROME CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000497000~MAPTARGET~J0051

6011000124106~MAPRULE~IFA 717823001 | Goldblatt syndrome |

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPTARGET~Q87.19

447562003~MAPGROUP~1

6011000124106~MAPTARGET~F79

6011000124106~MAPRULE~IFA 721089006 | Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome |

6011000124106~MAPRULE~IFA 721089006 | Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder) |

6011000124106~MAPADVICE~IF DENTINOGENESIS IMPERFECTA, SHORT STATURE, HEARING LOSS, INTELLECTUAL DISABILITY SYNDROME CHOOSE F78.A9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~CORRELATIONID~447561005

6011000124106~MAPADVICE~ALWAYS K00.5

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF DENTINOGENESIS IMPERFECTA, SHORT STATURE, HEARING LOSS, INTELLECTUAL DISABILITY SYNDROME CHOOSE H90.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE AND DENTINOGENESIS IMPERFECTA CHOOSE Q13.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~K00.5

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF DENTINOGENESIS IMPERFECTA, SHORT STATURE, HEARING LOSS, INTELLECTUAL DISABILITY SYNDROME CHOOSE Q87.19 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CHONDRODYSPLASIA, DENTINOGENESIS IMPERFECTA, JOINT LAXITY SYNDROME CHOOSE Q78.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 63890001 | Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (disorder) |

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF DENTINOGENESIS IMPERFECTA, SHORT STATURE, HEARING LOSS, INTELLECTUAL DISABILITY SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPADVICE~IF CHONDRODYSPLASIA, DENTINOGENESIS IMPERFECTA, JOINT LAXITY SYNDROME CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 63890001 | Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta |

6011000124106~MAPGROUP~4

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE AND DENTINOGENESIS IMPERFECTA CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q78.0

6011000124106~MAPADVICE~IF OSTEOGENESIS IMPERFECTA, TYPE IV B CHOOSE Q78.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF GOLDBLATT SYNDROME CHOOSE Q78.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CHONDRODYSPLASIA, DENTINOGENESIS IMPERFECTA, JOINT LAXITY SYNDROME CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q13.5

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~CORRELATIONID~447561005

6011000124106~MAPTARGET~Q74.8

6011000124106~MAPGROUP~3

6011000124106~MAPADVICE~IF OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE AND DENTINOGENESIS IMPERFECTA CHOOSE Q78.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~IF GOLDBLATT SYNDROME CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~2

6011000124106~MAPTARGET~K00.5

6011000124106~MAPTARGET~H90.5

6011000124106~MAPTARGET~Q78.9

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/422977003

http://purl.bioontology.org/ontology/SNOMEDCT/363070008

http://purl.bioontology.org/ontology/SNOMEDCT/11164009

http://purl.bioontology.org/ontology/SNOMEDCT/1148766007

http://purl.bioontology.org/ontology/SNOMEDCT/46557008

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MDRGER/10054013 MDRGER CUI
http://purl.bioontology.org/ontology/ICD10CM/K00.5 ICD10CM CUI
http://purl.bioontology.org/ontology/RCD/J0051 RCD CUI
http://purl.bioontology.org/ontology/MSHFRE/D003811 MSHFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/196286005 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDDRA/10054013 MEDDRA CUI
http://purl.bioontology.org/ontology/MESH/D003811 MESH CUI
http://purl.bioontology.org/ontology/NDFRT/N0000000935 NDFRT CUI
http://purl.bioontology.org/ontology/OMIM/MTHU036675 OMIM CUI
http://purl.bioontology.org/ontology/MDRFRE/10054013 MDRFRE CUI
http://purl.bioontology.org/ontology/SNMI/D4-51007 SNMI CUI
http://purl.org/obo/owl/HP#HP_0000703 BDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#3748 OCHV LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:0678 IFAR LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C07.793.700.270 RH-MESH LOOM
http://purl.bioontology.org/ontology/RCD/J0051 RCD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.850.800.270 RH-MESH LOOM
http://purl.obolibrary.org/obo/HP_0000703 HP LOOM
http://purl.obolibrary.org/obo/HP_0000703 UPHENO LOOM
http://purl.obolibrary.org/obo/HP_0000703 OBA LOOM
rgo:30122 GAMUTS LOOM
http://purl.jp/bio/4/id/200906070577749420 IOBC LOOM
http://purl.bioontology.org/ontology/MEDDRA/10054013 MEDDRA LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Dentinogenesis_Imperfecta CSEO LOOM
http://purl.obolibrary.org/obo/MONDO_0018849 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0018849 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018849 DOVES LOOM
http://purl.obolibrary.org/obo/NCIT_C84667 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D003811 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00039489 PMAPP-PMO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84667 NCIT LOOM
http://purl.bioontology.org/ontology/MESH/D003811 MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C07.650.800.270 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0005088 OMIT LOOM
http://www.orpha.net/ORDO/Orphanet_49042 ORDO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_10638 HRDO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_4154 NATPRO LOOM
http://purl.obolibrary.org/obo/DOID_4154 DTO LOOM
http://purl.obolibrary.org/obo/DOID_4154 DOID LOOM
http://purl.obolibrary.org/obo/DOID_4154 BAO LOOM
http://purl.obolibrary.org/obo/DOID_4154 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_4154 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_4154 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_4154 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_4154 FNS-H LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036675 OMIM LOOM
http://purl.bioontology.org/ontology/SNMI/D4-51007 SNMI LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0011436 OCHV LOOM
http://purl.bioontology.org/ontology/RCTV2/J005100 RCTV2 LOOM
http://www.gamuts.net/entity#dentinogenesis_imperfecta GAMUTS REST