| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | This syndrome is characterised by the association of toe syndactyly, facial dysmorphism including telecanthus (abnormal distance between the eyes) and a broad nasal tip, urogenital malformations and anal atresia. (Orphanet Rare Disease Ontology, Orphanet_140952) |
| External Link | http://www.omim.org/entry/300707 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the star syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FAM58A | family with sequence similarity 58, member A |
