Genopathy
Gene-Disorder Association · Article
Gene
MCFD2
Multiple Coagulation Factor Deficiency 2, ER Cargo Receptor Complex Subunit
Manually curated
Association Review

In brief

The association between MCFD2 (Multiple Coagulation Factor Deficiency 2, ER Cargo Receptor Complex Subunit) and Combined Deficiency Of Factor V And Factor Viii is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.

Sources 2
Clinical variants 0
Symptoms 18
Compounds 0
Trials 0
Publications 14
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

2 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
MCFD2

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Combined Deficiency Of Factor V And Factor Viii

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

18 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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07
Literature

Reading

14 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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08
Provenance

References & sources

13 references

Every source and publication cited across this dossier, as one numbered reference list.

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