Genopathy
Gene-Disorder Association · Article
Gene
KIF21A
Kinesin Family Member 21A
Manually curated
Association Review

In brief

The association between KIF21A (Kinesin Family Member 21A) and Neuromuscular Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 15
Compounds 0
Trials 0
Publications 0
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
KIF21A

The gene

1 source summary

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

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04
Neuromuscular Disease

The disorder

8 database identifiers

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

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05
Provenance

References & sources

3 references

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

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