OBO ID: DOID:0110786 |
Term Name: | hereditary spastic paraplegia 35 | Search Ontology: | |
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Definition: | A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. https://www.ncbi.nlm.nih.gov/pubmed/19068277 | ||
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Ontology: | Human Disease ( DOID:0110786 ) |
OTHER hereditary spastic paraplegia 35 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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