(Q18555032)

English

factor VII deficiency

Human disease

Factor VII deficiency
Factor VII deficiency (disorder)
deficiency, stable
Congenital proconvertin deficiency
Hypoproconvertinemia
F7 Deficiency

In more languages

Statements

class of disease

0 references

inherited blood coagulation disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

blood coagulation disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

autosomal recessive disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

health specialty

0 references

medical genetics

0 references

symptoms and signs

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

drug or therapy used for treatment

antihemophilic factor

1 reference

language of work or name

13 December 2016

genetic association

2 references

UniProt protein ID

13 August 2019

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000057593/MONDO_0009211

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

C98939

0 references

C131631

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

http://purl.obolibrary.org/obo/DOID_2215

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:2215

1 reference

Identifiers.org

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

http://purl.obolibrary.org/obo/HP_0008169

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

http://www.orpha.net/ORDO/Orphanet_327

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

C15.378.100.100.310

0 references

C15.378.100.141.310

0 references

C15.378.463.310

0 references

C16.320.099.310

0 references

0 references

PatientsLikeMe condition ID

factor-vii-deficiency

0 references

0 references

Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

GARD rare disease ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

Genetics Home Reference Conditions ID

factor-vii-deficiency

0 references

Human Phenotype Ontology ID

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

6 August 2018

Microsoft Academic ID

0 references

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

UniProt disease ID

0 references

WikiProjectMed ID

Factor VII deficiency

0 references

Sitelinks

Wikipedia(1 entry)

enwiki Factor VII deficiency

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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