OBO ID: DOID:0110796
Term Name: hereditary spastic paraplegia 44 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 44
  • SPG44
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42. https://www.ncbi.nlm.nih.gov/pubmed/19056803
References:
Ontology: Human Disease   (DOID:0110796)
OTHER hereditary spastic paraplegia 44 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GJC2 ?Spastic paraplegia 44, autosomal recessive 613206
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None