Synpolydactyly 1
| Disorder | |
|---|---|
| OMIM #: | #186000 (Click to access OMIM database) |
| Disorder: | Synpolydactyly 1 |
| Also known as: | SPD1 syndactyly, type II SDTY2 |
| Clinical | |
| Phenotype: | syndactyly of hands and feet, polydactyly of hands and feet |
| Seen In: |
Amish Old Order Mennonite Old Colony Mennonite Unknown/Other Mennonite Hutterite |
| Remarks: | Autosomal dominant |
| Mutations | |
| 1 Amish | |
| Gene: | HOXD13 |
| Base Change: | |
| Amino Acid Change: | |
| Last updated: | 2024-09-24 |
| References |
|---|
| Cross HE, Lerberg DB, McKusick VA. (1968) Type II syndactyly. Am J Hum Genet Jul;20(4):368-80. PubMed ID: 4298538 |
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