amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in UBQLN 2 gene located_in X chromosome. (Human Disease Ontology, DOID_0060206)
External Link http://www.omim.org/entry/300857
Similar Terms
Downloads & Tools

Genes

1 genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
UBQLN2 ubiquilin 2