hereditary spastic paraplegia 28

Term ID

DOID:0110779

Synonyms

autosomal recessive spastic paraplegia 28
autosomal recessive spastic paraplegia type 28
SPG28

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/23176821

References

ICD10CM:G11.4
MIM:609340
ORDO:101008

Ontology

Human Disease ( DOID:0110779 )

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