amyotrophic lateral sclerosis type 6
Go to external page http://purl.obolibrary.org/obo/MONDO_0011951
Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the FUS gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: FUS amyotrophic lateral sclerosis ALS6 amyotrophic lateral sclerosis 6, with or without frontotemporal dementia autosomal recessive amyotrophic lateral sclerosis 6 amyotrophic lateral sclerosis type 6 amyotrophic lateral sclerosis caused by mutation in FUS
Term information
- MESH:C567699 (MONDO:equivalentTo)
- GARD:9874 (OMIM:608030)
- DOID:0060198 (MONDO:equivalentTo)
- OMIM:608030 (MONDO:equivalentTo)
gard_rare, rare, nord_rare, clingen
https://omim.org/entry/608030
http://identifiers.org/mesh/C567699
http://purl.obolibrary.org/obo/DOID_0060198
https://rarediseases.info.nih.gov/diseases/9874/amyotrophic-lateral-sclerosis-type-6
https://search.clinicalgenome.org/kb/conditions/MONDO:0011951