Primary Ovarian Insufficiency 3
Disease ID: disease_node_17218
Connections displayed (default: 10).
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| Dbxref | MIM:608996 |
|---|---|
| Subclassof | DOID_0050736, DOID_5426 |
| Data Source | DOID |
| Doid Label | primary ovarian insufficiency 3 |
| Doid Description | A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17218 |
| Doid Id | DOID_0080860 |
| Label | Primary Ovarian Insufficiency 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Primary Ovarian Insufficiency(ID:disease_node_8834) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)