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A reference for what the literature reports. Not medical advice.

Disease

KIF5A-related neurological disorder

MONDO:0100629Mondo

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Findings

No curated finding names KIF5A-related neurological disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any nervous system disorder in which the cause of the disease is a variation in the KIF5A gene.

Definition from the Mondo Disease Ontology (MONDO:0100629), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: hereditary neurological disease
Narrower terms (3): autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
hereditary spastic paraplegia 10
myoclonus, intractable, neonatal