Disease #03585 (HPE11 (holoprosencephaly, type 11 (HPE-11)), OMIM:614226)
| Official abbreviation |
HPE11 |
| Name |
holoprosencephaly, type 11 (HPE-11) |
| OMIM ID |
614226 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
37 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
CDON |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|