Frontotemporal dementia and/or amyotrophic lateral sclerosis 7

Definition

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene.

Also known as amyotrophic lateral sclerosis caused by mutation in CHMP2B, amyotrophic lateral sclerosis, Chmp2B-related, CHMP2B amyotrophic lateral sclerosis, CHMP2B-related amyotrophic lateral sclerosis, frontotemporal dementia, chromosome 3-linked, FTD3 — per MONDO

Also identified as

• DOID 0060208 per MONDO
• DOID 0111227 per MONDO
• ICD9 331.19 per MONDO
• MESH C563708 per MONDO
• MESH C579991 per MONDO
• OMIM 600795 per MONDO
• OMIM 614696 per MONDO
• SCTID 702393003 per MONDO
• UMLS C1833296 per MONDO