| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C535563 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Absence of Tibia from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| THMA | Tibial hemimelia | 2.88009 |
