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Human Disease

hereditary spastic paraplegia 24

Term ID

DOID:0110775

Synonyms

autosomal recessive spastic paraplegia 24
autosomal recessive spastic paraplegia type 24
SPG24

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 13q14. https://www.ncbi.nlm.nih.gov/pubmed/12499481

References

GARD:9296
ICD10CM:G11.4
MIM:607584
ORDO:101004

Ontology

Human Disease ( DOID:0110775 )

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