| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Amish lethal microcephaly is a very rare syndrome characterized by extreme microcephaly and early death, within the first year. (Orphanet Rare Disease Ontology, Orphanet_99742) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C538247 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Amish lethal microcephaly from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| SLC25A19 | solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 | 2.88009 |
