Disease #00654 (HH5 (hypogonadism, hypogonadotropic, type 5 with/without anosmia (HH-5)), OMIM:612370)
| Official abbreviation |
HH5 |
| Name |
hypogonadism, hypogonadotropic, type 5 with/without anosmia (HH-5) |
| OMIM ID |
612370 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CHD7 |
| 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
|