Disease #00131
| Official abbreviation |
HSCR1 |
| Name |
Hirschsprung disease, susceptibility to, 1 |
| OMIM ID |
142623 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
RET |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|