| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Underdevelopment of the helix that either affects the entire helix, or is localized. (Human Phenotype Ontology, HP_0008577) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008577 |
| Similar Terms | |
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1 genes associated with the underfolded helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC6A8 | solute carrier family 6 (neurotransmitter transporter), member 8 |
