| Disease ID | Source | Name | Description |
| 601680 | OMIM | Arthrogryposis, distal, 2B1 (DA2B1) | A form of distal arthrogryposis, a disease characterized by congenital joint contractures that mainly involve two or more distal parts of the limbs, in the absence of a primary neurological or muscle disease. DA2B is characterized by contractures of the hands and feet, and a distinctive face characterized by prominent nasolabial folds, small mouth and downslanting palpebral fissures. DA2B1 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry. |