(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

default for all languages

No label defined

No description defined

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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