hereditary spastic paraplegia 27

Term ID

DOID:0110778

Synonyms

autosomal recessive spastic paraplegia 27
autosomal recessive spastic paraplegia type 27
SPG27

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 10q22.1-q24.1. https://www.ncbi.nlm.nih.gov/pubmed/15455396

References

ICD10CM:G11.4
MIM:609041
ORDO:101007

Ontology

Human Disease ( DOID:0110778 )

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