| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Chronic loss of joint motion in the thumb due to structural changes in non-bony tissue. The term camptodactyly is used if the distal and/or proximal interphalangeal joints are affected. (Human Phenotype Ontology, HP_0009600) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009600 |
| Similar Terms | |
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3 genes associated with the flexion contracture of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
