OBO ID: DOID:0110801
Term Name: hereditary spastic paraplegia 49 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 49
  • autosomal recessive spastic paraplegia type 49
  • SPG49
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32. https://www.ncbi.nlm.nih.gov/pubmed/23176824
References:
Ontology: Human Disease   (DOID:0110801)
OTHER hereditary spastic paraplegia 49 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TECPR2 Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay 615031
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None