Genopathy
Gene-Disorder Association · Article
Gene
LOC109504728
Chromosome 9 Open Reading Frame 72 Repeat Instability Region
Disorder
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1
First reported 1953
Supporting publications 10
Key publication · disorder Progressive bulbar paralysis showing heredofamilial incidence and intellectual impairment.A.M.A. archives of neurology and psychiatry · 1953
Association Review

In brief

The association between LOC109504728 (Chromosome 9 Open Reading Frame 72 Repeat Instability Region) and Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 0
Symptoms 58
Compounds 0
Trials 0
Publications 10
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
LOC109504728

The gene

1 source summary

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

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04
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1

The disorder

16 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

43 clinical features

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

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06
Literature

Reading

10 publications

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

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07
Provenance

References & sources

15 references

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

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