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ZIRC
OBO ID: DOID:0110818
Term Name: hereditary spastic paraplegia 73 Search Ontology:
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)
OTHER hereditary spastic paraplegia 73 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CPT1C ?Spastic paraplegia 73, autosomal dominant 616282
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None