hereditary spastic paraplegia 23

Term ID

DOID:0110774

Synonyms

• Lison syndrome
• Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
• spastic paraplegia 23
• spastic paraplegia with pigmentary abnormalities
• SPG23

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32. https://www.ncbi.nlm.nih.gov/pubmed/14681889

References

• GARD:336
• ICD10CM:G11.4
• OMIM:270750
• ORDO:101003

Ontology

Human Disease   ( DOID:0110774 )