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Human Disease

hereditary spastic paraplegia 14

Term ID

DOID:0110767

Synonyms

autosomal recessive spastic paraplegia 14
autosomal recessive spastic paraplegia type 14
SPG14

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 3q27-q28. https://www.ncbi.nlm.nih.gov/pubmed/10877981

References

GARD:9589
ICD10CM:G11.4
MIM:605229
ORDO:100995

Ontology

Human Disease ( DOID:0110767 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

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Alliance (1)

Genes Involved

Zebrafish Models