OBO ID: DOID:0110825
Term Name: hereditary spastic paraplegia 9B Search Ontology:
Synonyms:
  • autosomal recessive complex spastic paraplegia type 9B
  • autosomal recessive spastic paraplegia 9B
  • SPG9B
Definition: A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.https://www.ncbi.nlm.nih.gov/pubmed/26026163
References:
Ontology: Human Disease   (DOID:0110825)
Relationships
is a type of:
OTHER hereditary spastic paraplegia 9B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ALDH18A1 Spastic paraplegia 9B, autosomal recessive 616586
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None