duodenal atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in complete obliteration of the duodenal lumen, that is, an abnormal closure of the duodenum. (Human Phenotype Ontology, HP_0002247)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002247
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Genes

7 genes associated with the duodenal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CEP57 centrosomal protein 57kDa
CHD7 chromodomain helicase DNA binding protein 7
FOXF1 forkhead box F1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
RFX6 regulatory factor X, 6
SALL1 spalt-like transcription factor 1
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E