hereditary spastic paraplegia 73

Term ID

DOID:0110818

Synonyms

autosomal dominant spastic paraplegia 73
autosomal dominant spastic paraplegia type 73
SPG73

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/25751282

References

ICD10CM:G11.4
MIM:616282
ORDO:444099

Ontology

Human Disease ( DOID:0110818 )

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