Donnai-Barrow syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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1 genes/proteins associated with the disease Donnai-Barrow syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LRP2 low density lipoprotein receptor-related protein 2 2.88009