Disease #03754 (HH14 (hypogonadism, hypogonadotropic, type 14 with/without anosmia (HH14)), OMIM:614858)
| Official abbreviation |
HH14 |
| Name |
hypogonadism, hypogonadotropic, type 14 with/without anosmia (HH14) |
| OMIM ID |
614858 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
WDR11 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-03-01 13:14:05 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|