| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | GRACILE syndrome is an inherited lethal mitochondrial disorder characterized by fetal growth restriction (GR), aminoaciduria (A), cholestasis (C), iron overload (I), lactacidosis (L), and early death (E). (Orphanet Rare Disease Ontology, Orphanet_53693) |
| External Link | http://www.omim.org/entry/603358 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the gracile syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| BCS1L | BC1 (ubiquinol-cytochrome c reductase) synthesis-like |
