OBO ID: DOID:0110813
Term Name: hereditary spastic paraplegia 62 Search Ontology:
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
is a type of:
OTHER hereditary spastic paraplegia 62 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ERLIN1 Spastic paraplegia 62 615681
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None