(Q5160407)

English

congenital afibrinogenemia

Human disease

Factor I deficiency
Fibrinogen deficiency
Afibrinogenemia
CAFBN

In more languages

Statements

class of disease

0 references

Factor I Deficiency

0 references

inherited blood coagulation disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

autosomal recessive disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

blood coagulation disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

health specialty

0 references

genetic association

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000171557/Orphanet_98880

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/ENSG00000171564/Orphanet_98880

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C98130

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

equivalent class

http://purl.obolibrary.org/obo/DOID_0050878

1 reference

Disease Ontology

4 February 2016

https://raw.githubusercontent.com/DiseaseOntology/HumanDiseaseOntology/9b96f2e36e01ad4cf87c5cef1ac0c2e8708157d6/src/ontology/doid.owl

http://identifiers.org/doid/DOID:0050878

1 reference

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

http://purl.obolibrary.org/obo/DOID_2236

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:2236

1 reference

Identifiers.org

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

http://purl.obolibrary.org/obo/DOID_0050878

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0050878

1 reference

Identifiers.org

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

Identifiers

MeSH descriptor ID

subject named as

Afibrinogenemia

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

C15.378.100.100.056

0 references

C15.378.100.141.072

0 references

C15.378.463.067

0 references

C16.320.099.056

0 references

1 reference

imported from Wikimedia project

English Wikipedia

PatientsLikeMe condition ID

congenital-afibrinogenemia

0 references

0 references

1 reference

Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

1 reference

imported from Wikimedia project

English Wikipedia

0 references

Encyclopædia Britannica Online ID

science/afibrinogenemia

subject named as

afibrinogenemia

0 references

GARD rare disease ID

1 reference

Genetic and Rare Diseases Information Center

1 April 2019

Genetics Home Reference Conditions ID

congenital-afibrinogenemia

0 references

1 reference

imported from Wikimedia project

English Wikipedia

afibrinogenemia

0 references

Microsoft Academic ID

0 references

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

26 January 2022

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

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

UniProt disease ID

0 references

WikiProjectMed ID

Congenital afibrinogenemia

0 references

Sitelinks

Wikipedia(4 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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