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
MIM:611945
ORDO:171612

Ontology

Human Disease ( DOID:0110788 )

Relationships

is a type of: autosomal dominant disease hereditary spastic paraplegia

autosomal dominant disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models