Primary Ovarian Insufficiency 10
Disease ID: disease_node_17211
Connections displayed (default: 10).
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| Dbxref | MIM:612885 |
|---|---|
| Subclassof | DOID_5426, DOID_0050737 |
| Data Source | DOID |
| Doid Label | primary ovarian insufficiency 10 |
| Doid Description | A primary ovarian insufficiency that is characterized by primary amenorrhea, hypergonadotropic ovarian insufficiency, and genomic instability in somatic cells and that has_material_basis_in homozygous mutation in the MCM8 gene on chromosome 20p. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17211 |
| Doid Id | DOID_0080867 |
| Label | Primary Ovarian Insufficiency 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Primary Ovarian Insufficiency(ID:disease_node_8834) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)