Hirschsprung's disease is a blockage of the large intestine. It occurs due to poor muscle movement in the bowel. It is a congenital condition, which means it is present from birth.
Gene Name | Chromosome number | BMRB Entries | PDB Entries |
---|---|---|---|
GDNF | 5 | PDB Entries | |
PCM1 | 8 | ||
PRKDC | 8 | ||
RET | 10 | BMRB Entries | PDB Entries |