hereditary spastic paraplegia 2

Term ID

DOID:0110773

Synonyms

• spastic paraplegia type 2
• SPG2
• X-linked spastic paraplegia 2

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2. https://www.ncbi.nlm.nih.gov/pubmed/8012387

References

• GARD:4923
• ICD10CM:G11.4
• OMIM:312920
• ORDO:99015

Ontology

Human Disease   ( DOID:0110773 )