OBO ID: DOID:0060206 |
Term Name: | amyotrophic lateral sclerosis type 15 | Search Ontology: | |
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Synonyms: |
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Definition: | An amyotrophic lateral sclerosis that has_material_basis_in mutation in the UBQLN2 gene on chromosome X. (2) | ||
References: | |||
Ontology: | Human Disease ( DOID:0060206 ) |
OTHER amyotrophic lateral sclerosis type 15 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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UBQLN2 | Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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