Primary Ovarian Insufficiency 19
Disease ID: disease_node_17222
Connections displayed (default: 10).
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| Dbxref | MIM:619245 |
|---|---|
| Subclassof | DOID_5426, DOID_0050737 |
| Data Source | DOID |
| Synonyms | POF19, POI19, premature ovarian failure 19 |
| Doid Label | primary ovarian insufficiency 19 |
| Doid Description | A primary ovarian insufficiency characterized by irregular menses that cease in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the HSF2BP gene on chromosome 21q22. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17222 |
| Doid Id | DOID_0112278 |
| Label | Primary Ovarian Insufficiency 19 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Primary Ovarian Insufficiency(ID:disease_node_8834) (Disease)