| Dataset | ClinVar Gene-Phenotype Associations 2025 |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities. (Human Disease Ontology, DOID_11569) |
| External Link | http://www.omim.org/entry/604715 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the Neurocirculatory asthenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
| Symbol | Name |
|---|---|
| SLC6A2 | solute carrier family 6 (neurotransmitter transporter), member 2 |
