Genopathy
Gene-Disorder Association · Article
Gene
LMAN1
Lectin, Mannose Binding 1
Disorder
Hemophilia A
First reported 2004
Supporting publications 3
Key publication · gene–disorder A mutation in LMAN1 (ERGIC-53) causing combined factor V and factor VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia.Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis · 2004
Key publication · disorder The Consumption of Prothrombin during Coagulation: The Defect in Haemophilia and Thrombo-Cytopenic Purpura.Journal of clinical pathology · 1950
Manually curated
Association Review

In brief

The association between LMAN1 (Lectin, Mannose Binding 1) and Hemophilia A is reported, with clinical genetic testing available.

Sources 1
Clinical variants 1
Symptoms 60
Compounds 0
Trials 0
Publications 3
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

1 source

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

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03
LMAN1

The gene

1 source summary

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

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04
Hemophilia A

The disorder

18 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

50 clinical features

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

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06
ClinVar and variant evidence

Genetic basis

1 clinical variant

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

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

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08
Literature

Reading

3 publications

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

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09
Provenance

References & sources

10 references

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

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