Search Ontology:
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
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Genes Involved
Zebrafish Models
Citations