| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A hypogonadism that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. (Human Disease Ontology, DOID_14447) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D006059 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Gonadal Dysgenesis from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| FMR1 | fragile X mental retardation 1 | 2.88009 |
