dental enamel hypoplasia (Q5375191)

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Human disease

• Enamel Hypoplasia
• Enamel hypoplasia (disorder)

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Language	Label	Description	Also known as
English	dental enamel hypoplasia	Human disease	Enamel Hypoplasia Enamel hypoplasia (disorder)

Statements

instance of

class of disease

0 references

subclass of

teeth hard tissue disease

1 reference

stated in

Disease Ontology

retrieved

29 November 2021

Disease Ontology ID

DOID:693

image

법랑질저형성증.jpg
250 × 178; 19 KB

0 references

health specialty

dentistry

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

WordLift URL

http://data.wordlift.io/wl01714/entity/enamel-hypoplasia.html

1 reference

reference URL

https://fr.dentist/kb/enamel-hypoplasia/

NCI Thesaurus ID

C34529

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:693

exact match

http://purl.obolibrary.org/obo/DOID_693

1 reference

stated in

Disease Ontology

retrieved

29 November 2021

Disease Ontology ID

DOID:693

http://identifiers.org/doid/DOID:693

1 reference

stated in

Identifiers.org

reference URL

https://registry.identifiers.org/registry/doid

http://purl.obolibrary.org/obo/HP_0006297

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0006297

Commons category

Enamel hypoplasia

0 references

Identifiers

MeSH descriptor ID

D003744

mapping relation type

exact match

subject named as

Dental Enamel Hypoplasia

1 reference

Mondo ID

MONDO_0004038

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

MeSH tree code

C07.650.800.295.625

0 references

C07.793.700.295.625

0 references

C16.131.850.800.295.625

0 references

Disease Ontology ID

DOID:693

1 reference

stated in

Disease Ontology

retrieved

29 November 2021

Disease Ontology ID

DOID:693

Experimental Factor Ontology ID

1001304

1 reference

based on heuristic

inferred by common MONDO mappings on source and on Wikidata

Human Phenotype Ontology ID

HP:0006297

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0006297

ICD-10 ID

K00.4

1 reference

imported from Wikimedia project

English Wikipedia

ICD-11 ID (Foundation)

701425154

0 references

ICD-9 ID

520.4

1 reference

imported from Wikimedia project

English Wikipedia

Medical Dictionary for Regulatory Activities ID

10044030

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

Microsoft Academic ID

2776462190

0 references

Mondo ID

MONDO_0004038

0 references

OpenAlex ID

C2776462190

1 reference

stated in

OpenAlex

retrieved

26 January 2022

reference URL

https://docs.openalex.org/download-snapshot/snapshot-data-format

UMLS CUI

C0011351

2 references

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:693

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0006297

C4280456

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0006297

C4280457

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0006297

C1851854

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0006297

 

Sitelinks

Wikipedia(3 entries)

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• arwiki نقص تنسج الميناء
• enwiki Enamel hypoplasia
• kowiki 법랑질 저형성증

Wikibooks(0 entries)

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Wikinews(0 entries)

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Wikiquote(0 entries)

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Wikisource(0 entries)

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Wikiversity(0 entries)

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Wikivoyage(0 entries)

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Wiktionary(0 entries)

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Multilingual sites(1 entry)

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• commonswiki Category:Enamel hypoplasia

Retrieved from "https://www.wikidata.org/w/index.php?title=Q5375191&oldid=2252155543"