Amyotrophic lateral sclerosis (ALS14)
GPTKB entity
Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurodegenerative disease
genetic disorder |
| gptkbp:affects |
gptkb:nervous_system
motor neurons |
| gptkbp:alternativeName |
ALS14
VCP-related ALS |
| gptkbp:associatedWith |
gptkb:VCP
|
| gptkbp:hasGeneticAlteration |
VCP gene mutation
|
| https://www.w3.org/2000/01/rdf-schema#label |
Amyotrophic lateral sclerosis (ALS14)
|
| gptkbp:ICD-10_code |
G12.2
|
| gptkbp:inheritance |
autosomal dominant
familial |
| gptkbp:OMIM |
614808
|
| gptkbp:onset |
adult
|
| gptkbp:subspecies |
gptkb:Amyotrophic_lateral_sclerosis
|
| gptkbp:symptom |
muscle atrophy
muscle weakness fasciculations dysphagia dysarthria |
| gptkbp:bfsParent |
gptkb:VCP
|
| gptkbp:bfsLayer |
7
|