(Q56013659)

English

hypomaturation amelogenesis imperfecta

human disease

Amelogenesis imperfecta type 2

In more languages

Statements

class of disease

0 references

amelogenesis imperfecta

0 references

genetic association

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000125363/Orphanet_100033

based on heuristic

inferred from an Open Targets association score over 0.7

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000137674/Orphanet_100033

based on heuristic

inferred from an Open Targets association score over 0.7

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000166415/Orphanet_100033

based on heuristic

inferred from an Open Targets association score over 0.7

520.5

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

http://www.orpha.net/ORDO/Orphanet_100033

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

GARD rare disease ID

1 reference

Genetic and Rare Diseases Information Center

1 April 2019

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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