Ovarian Dysgenesis 1
Disease ID: disease_node_14944
Connections displayed (default: 10).
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| Dbxref | MIM:233300 |
|---|---|
| Subclassof | DOID_14450, DOID_0050737 |
| Data Source | DOID |
| Doid Label | ovarian dysgenesis 1 |
| Doid Description | A 46 XX gonadal dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_14944 |
| Doid Id | DOID_0080493 |
| Label | Ovarian Dysgenesis 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Gonadal Dysgenesis, 46,Xx(ID:disease_node_10923) (Disease)