OBO ID: DOID:0110779
Term Name: hereditary spastic paraplegia 28 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 28
  • autosomal recessive spastic paraplegia type 28
  • SPG28
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/23176821
References:
Ontology: Human Disease   (DOID:0110779)
OTHER hereditary spastic paraplegia 28 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DDHD1 Spastic paraplegia 28, autosomal recessive 609340
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None