hereditary spastic paraplegia 49

Term ID

DOID:0110801

Synonyms

autosomal recessive spastic paraplegia 49
autosomal recessive spastic paraplegia type 49
SPG49

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32. https://www.ncbi.nlm.nih.gov/pubmed/23176824

References

ICD10CM:G11.4
MIM:615031
ORDO:320385

Ontology

Human Disease ( DOID:0110801 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models