OBO ID: DOID:0110783
Term Name: hereditary spastic paraplegia 32 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 32
  • autosomal recessive spastic paraplegia type 32
  • SPG32
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21. https://www.ncbi.nlm.nih.gov/pubmed/17515546
References:
Ontology: Human Disease   (DOID:0110783)
OTHER hereditary spastic paraplegia 32 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None