Feingold Syndrome

About the Disease
Feingold Syndrome 1, also known as feingold syndrome, is related to duodenal atresia and esophageal atresia. An important gene associated with Feingold Syndrome 1 is MYCN (MYCN Proto-Oncogene, BHLH Transcription Factor), and among its related pathways/superpathways are Cell differentiation - expanded index and miRNAs involvement in the immune response in sepsis. Affiliated tissues include small intestine, bone and kidney, and related phenotypes are microcephaly and brachydactyly

Common Targets
GNAO1 | COMP | MYCN | SLC26A4

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