|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital form of torticollis resulting from shortening of the sternocleidomastoid muscle and leading to a limited range of motion in both rotation and lateral bending. (Human Phenotype Ontology, HP_0005988)|
|Downloads & Tools|
6 genes associated with the congenital muscular torticollis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.