Disease #02985 (HPE7 (holoprosencephaly, type 7 (HPE-7)), OMIM:610828)
| Official abbreviation |
HPE7 |
| Name |
holoprosencephaly, type 7 (HPE-7) |
| OMIM ID |
610828 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
PTCH1 |
| 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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|