| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Tibial hemimelia is a rare congenital anomaly characterized by deficiency of the tibia with a relatively intact fibula. (Orphanet Rare Disease Ontology, Orphanet_93322) |
| External Link | http://www.omim.org/entry/275220 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the ?tibial hemimelia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| THM | thymoma |
