Disease #07148 (HH (hypogonadotropic hypogonadism))
| Official abbreviation |
HH |
| Name |
hypogonadotropic hypogonadism |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
TCF12 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2025-01-23 09:27:10 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|