familial amyotrophic lateral sclerosis

instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome

Wikidata entity: Q55345644

P2293 genetic association ... Q15328137 (SOD1) SOD1
P2293 genetic association ... Q17913377 (DCTN1) DCTN1
P2293 genetic association ... Q18032318 (VCP) VCP
P2293 genetic association ... Q18035056 (OPTN) OPTN
P2293 genetic association ... Q18037179 (TARDBP) TARDBP
P279 subclass of ... Q206901 (amyotrophic lateral sclerosis) amyotrophic lateral sclerosis
P279 subclass of ... Q19001236 (nervous system heredodegenerative disease) nervous system heredodegenerative disease
External Ids
P11956Experimental Factor Ontology ID0001356
P5270Mondo IDMONDO_0005144

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