OBO ID: DOID:0060209 |
Term Name: | amyotrophic lateral sclerosis type 18 | Search Ontology: | |
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Definition: | An amyotrophic lateral sclerosis that has_material_basis_in mutation in the PFN1 gene on chromosome 17. (2) | ||
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Ontology: | Human Disease ( DOID:0060209 ) |
OTHER amyotrophic lateral sclerosis type 18 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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