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ZIRC
OBO ID: DOID:0110789
Term Name: hereditary spastic paraplegia 38 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 38
  • autosomal dominant spastic paraplegia type 38
  • SPG38
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15.https://www.ncbi.nlm.nih.gov/pubmed/18401025
References:
Ontology: Human Disease   (DOID:0110789)
OTHER hereditary spastic paraplegia 38 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPG38 Spastic paraplegia 38, autosomal dominant 612335
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None