Search Ontology:
Human Disease

hereditary spastic paraplegia 62

Term ID
DOID:0110813
Synonyms
  • autosomal recessive spastic paraplegia 62
  • autosomal recessive spastic paraplegia type 62
  • SPG62
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References
Ontology
Human Disease   ( DOID:0110813 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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