|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Underdevelopment of the helix that either affects the entire helix, or is localized. (Human Phenotype Ontology, HP_0008577)|
|Downloads & Tools|
1 genes associated with the underfolded helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SLC6A8||solute carrier family 6 (neurotransmitter transporter), member 8|