Query author contributions in Reactome
Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.
If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.
Details on Person syndactyly
| Class:Id | Disease:2071917 |
|---|---|
| _displayName | syndactyly |
| _timestamp | 2012-01-26 20:54:53 |
| created | [InstanceEdit:2071916] Rothfels, K, 2012-01-26 |
| definition | A synostosis that results_in the fusion of two or more digits. |
| identifier | 11193 |
| name | syndactyly |
| referenceDatabase | [ReferenceDatabase:1247631] DOID |
| synonym | Symphalangism Symphalangy (disorder) (Polysyndactyly) or (symphalangism) or (syndactyly NOS) Webbing of digits |
| (disease) | [EntityWithAccessionedSequence:2071931] FGFR2c A315S [plasma membrane] [Homo sapiens] [Complex:2071933] FGFR2c A315S mutant dimer [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:2071942] p-8Y-FGFR2c A315S mutant [plasma membrane] [Homo sapiens] [Complex:2071951] p-8Y-FGFR2c A315S dimer [plasma membrane] [Homo sapiens] [Complex:2071955] p-8Y-FGFR2c A314D dimer [plasma membrane] [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by syndactyly (2071917)
