Search Ontology:
Human Disease

hereditary spastic paraplegia 73

Term ID
DOID:0110818
Synonyms
  • autosomal dominant spastic paraplegia 73
  • autosomal dominant spastic paraplegia type 73
  • SPG73
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/25751282
References
Ontology
Human Disease   ( DOID:0110818 )
Relationships
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Genes Involved
Zebrafish Models