Search Ontology:
Human Disease

hereditary spastic paraplegia 18

Term ID
DOID:0110771
Synonyms
  • autosomal recessive spastic paraplegia 18
  • autosomal recessive spastic paraplegia type 18
  • IDMDC
  • intellectual disability, motor dysfunction and joint contractures
  • SPG18
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11. https://www.ncbi.nlm.nih.gov/pubmed/21330303
References
Ontology
Human Disease   ( DOID:0110771 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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