hirschsprung's disease Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel. (Human Disease Ontology, DOID_10487)
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Genes

13 genes involed in the disease hirschsprung's disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CCDC6 coiled-coil domain containing 6
ECE1 endothelin converting enzyme 1
EDN3 endothelin 3
EDNRB endothelin receptor type B
GDNF glial cell derived neurotrophic factor
KIF1BP KIF1 binding protein
L1CAM L1 cell adhesion molecule
NRG1 neuregulin 1
NRTN neurturin
PCM1 pericentriolar material 1
RET ret proto-oncogene
SOX10 SRY (sex determining region Y)-box 10
ZEB2 zinc finger E-box binding homeobox 2