slurred speech Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal coordination of muscles involved in speech. (Human Phenotype Ontology, HP_0001350)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001350
Similar Terms
Downloads & Tools

Genes

7 genes associated with the slurred speech phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
CA8 carbonic anhydrase VIII
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
GLB1 galactosidase, beta 1
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
NEU1 sialidase 1 (lysosomal sialidase)
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3