| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A chronic loss of wrist joint motion due to structural changes in muscle, tendons, ligaments, or skin that prevent normal movement of the joints of the wrist. (Human Phenotype Ontology, HP_0001239) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0001239 |
| Similar Terms | |
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8 genes associated with the wrist flexion contracture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
