hereditary spastic paraplegia 30

Term ID

DOID:0110781

Synonyms

• autosomal dominant spastic paraplegia 30
• autosomal recessive spastic paraplegia 30
• autosomal spastic paraplegia type 30
• SPG30

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37. (2)

References

• ICD10CM:G11.4
• OMIM:610357
• ORDO:101010

Ontology

Human Disease   ( DOID:0110781 )