|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Donnai-Barrow syndrome (DBS) is a rare, often severe, multiple congenital malformation syndrome with typical facial dysmorphism, ocular findings, hearing loss, agenesis of the corpus callosum, and variable intellectual disability. Congenital diaphragmatic hernia (CDH) and/or omphalocele are common (see these terms). (Orphanet Rare Disease Ontology, Orphanet_2143)|
|Downloads & Tools|
1 genes/proteins associated with the disease Donnai-Barrow syndrome from the curated CTD Gene-Disease Associations dataset.
|LRP2||low density lipoprotein receptor-related protein 2||2.88009|