OBO ID: DOID:0110817 |
Term Name: | hereditary spastic paraplegia 72A | Search Ontology: | |
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Definition: | A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2. https://www.ncbi.nlm.nih.gov/pubmed/24388663 | ||
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Ontology: | Human Disease ( DOID:0110817 ) |
OTHER hereditary spastic paraplegia 72A PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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