inherited primary ovarian failure
MONDO:0019852Mondo
Findings
No curated finding names inherited primary ovarian failure yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0019852), read 2026-09-29. CC BY 4.0.
Genes
5 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ANKRD31HGNC:26853
- Strong · PanelApp Australia · Autosomal dominant · 2025
- NR5A1HGNC:7983
- Strong · PanelApp Australia · Autosomal dominant · 2025
- LHX8HGNC:28838
- Limited · PanelApp Australia · Autosomal dominant · 2025
- SOHLH2HGNC:26026
- Limited · PanelApp Australia · Autosomal dominant · 2025
- TUFMHGNC:12420
- Limited · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
- Narrower terms (41)
- 46 XX gonadal dysgenesis
- 46,XX ovarian dysgenesis-short stature syndrome
- aromatase deficiency
- ataxia telangiectasia
- blepharophimosis, ptosis, and epicanthus inversus syndrome
- classic galactosemia
- congenital lipoid adrenal hyperplasia due to STAR deficency
- osteosclerosis-ichthyosis-premature ovarian failure syndrome
- Perrault syndrome
- premature ovarian failure 1
- premature ovarian failure 10
- premature ovarian failure 11
- premature ovarian failure 12
- premature ovarian failure 13
- premature ovarian failure 14
- premature ovarian failure 15
- premature ovarian failure 16
Other names
4 names
Resolves to: inherited primary ovarian failure
- Also called
- hereditary primary ovarian failureinherited POIinherited premature ovarian failureinherited primary ovarian insufficiency