Disease #00900 (Central hypoventilation syndrome, congenital, with or without Hirschsprung disease (Haddad syndrome), OMIM:209880)
| Official abbreviation |
- |
| Name |
Central hypoventilation syndrome, congenital, with or without Hirschsprung disease (Haddad syndrome) |
| OMIM ID |
209880 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 6 genes |
ASCL1, BDNF, EDN3, GDNF, PHOX2B, RET |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
