OBO ID: DOID:0110780
Term Name: hereditary spastic paraplegia 29 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 29
  • SPG29
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. https://www.ncbi.nlm.nih.gov/pubmed/16130112
References:
Ontology: Human Disease   ( DOID:0110780 )
Relationships
is a type of:
OTHER hereditary spastic paraplegia 29 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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