hereditary spastic paraplegia 15

Term ID

DOID:0110768

Synonyms

• autosomal recessive spastic paraplegia 15
• autosomal recessive spastic paraplegia type 15
• hereditary spastic paraparesis type 15
• Kjellin syndrome
• spastic paraplegia and retinal degeneration
• spastic paraplegia-retinal degeneration syndrome
• SPG15

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1. https://www.ncbi.nlm.nih.gov/pubmed/18394578

References

• GARD:9581
• ICD10CM:G11.4
• OMIM:270700
• ORDO:100996

Ontology

Human Disease   ( DOID:0110768 )