dysphagia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Difficulty in swallowing. (Human Phenotype Ontology, HP_0002015)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003158
Similar Terms
Downloads & Tools

Genes

3 gene mutations causing the dysphagia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
COL19A1 collagen, type XIX, alpha 1
LDB3 LIM domain binding 3