amyotrophic lateral sclerosis 19 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in ERBB4 gene located_in chromosome 2. (Human Disease Ontology, DOID_0060210)
External Link http://www.omim.org/entry/615515
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Genes

1 genes associated with the amyotrophic lateral sclerosis 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ERBB4 erb-b2 receptor tyrosine kinase 4