Disease name | Hirschsprung Disease |
---|---|
Classfication | Gastrointestinal system disease |
Related Enzyme(s) | |
EFO | Orphanet:388 |
DOID | 10487 |
OMIM | |
NCI | |
Definition | A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel. |
Gene symbol | Species | Enzyme | Editing site(s) | Editing Type | PMID | RADAR | REDIportal | Description |
---|---|---|---|---|---|---|---|---|
EDNRB | Human | ADAR1;ADAR2 | 1 | A-to-I | When ETB proteins are functionally altered by mutation, it may lead to HSCR. The sequence of the mutant cDNA shows a nucleotide substitution from A to G at position 950, resulting in the conversion from glutamine to arginine. |