Genopathy
Gene-Disorder Association · Article
Gene
FTL
Ferritin Light Chain
Disorder
Movement Disease
First reported 2006
Supporting publications 1
Key publication · gene–disorder Characterization of the l-ferritin variant 460InsA responsible of a hereditary ferritinopathy disorder.Neurobiology of disease · 2006
Key publication · disorder [The late result of surgery of extrapyramidal movement disorders and paraplegias].Deutsche Zeitschrift fur Nervenheilkunde · 1952
Manually curated
Association Review

In brief

The association between FTL (Ferritin Light Chain) and Movement Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 28
Compounds 0
Trials 0
Publications 1
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
FTL

The gene

1 source summary

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

Request access
04
Movement Disease

The disorder

6 database identifiers

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

Request access
05
Literature

Reading

1 publication

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

Request access
06
Provenance

References & sources

4 references

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

Request access