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
|
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