eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hirschsprung disease |
| Comorbidity | C1736133|congenital central hypoventilation syndrome |
| Sentences | 3 |
| PubMedID- 24135798 | An unusual cause of fetal hypomobility:congenital central hypoventilation syndrome associated with hirschsprung disease. |
| PubMedID- 23427517 | congenital central hypoventilation syndrome with hirschsprung's disease due to phox2b gene mutation in a turkish infant. |
| PubMedID- 21286029 | congenital central hypoventilation syndrome with hirschsprung's disease, also known as haddad syndrome, is an extremely rare disorder with variable symptoms. |
Page: 1