hereditary spastic paraplegia 37

Term ID

DOID:0110788

Synonyms

• autosomal dominant spastic paraplegia 37
• autosomal dominant spastic paraplegia type 37
• SPG37

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3. https://www.ncbi.nlm.nih.gov/pubmed/17605047

References

• ICD10CM:G11.4
• OMIM:611945
• ORDO:171612

Ontology

Human Disease   ( DOID:0110788 )