OBO ID: DOID:0060193 |
Term Name: | amyotrophic lateral sclerosis type 1 | Search Ontology: | |
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Synonyms: |
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Definition: | An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis | ||
References: |
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Ontology: | Human Disease ( DOID:0060193 ) |
OTHER amyotrophic lateral sclerosis type 1 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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DCTN1 | {Amyotrophic lateral sclerosis, susceptibility to} | 105400 | |
PRPH | {Amyotrophic lateral sclerosis, susceptibility to} | 105400 | |
SOD1 | Amyotrophic lateral sclerosis 1 | 105400 | |
NEFH | {?Amyotrophic lateral sclerosis, susceptibility to} |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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