| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism. (Human Disease Ontology, DOID_0060237) |
| External Link | https://www.disgenet.org/browser/0/1/0/C3280203 |
| Similar Terms | |
| Downloads & Tools |
3 genes associated with the disease Warburg Micro Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
