Search Ontology:

Human Disease

hereditary spastic paraplegia 36

Term ID

DOID:0110787

Synonyms

autosomal dominant spastic paraplegia 36
autosomal dominant spastic paraplegia type 36
SPG36

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24. https://www.ncbi.nlm.nih.gov/pubmed/19357379

References

ICD10CM:G11.4
OMIM:613096
ORDO:320365

Ontology

Human Disease ( DOID:0110787 )

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

Citations