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Disease association ontology term - MONDO:0010936 - frontotemporal dementia and/or amyotrophic lateral sclerosis 7

Term summary

ID
MONDO:0010936
Name
frontotemporal dementia and/or amyotrophic lateral sclerosis 7
Ontology or CV name
Disease association
Definition
Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene.

Parents

Annotation

Disease association

MONDO:0010936 - frontotemporal dementia and/or amyotrophic lateral sclerosis 7

References:

Genes: