An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]
Synonyms: hereditary primary ovarian failure inherited premature ovarian failure
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:19294 (Orphanet:95710)
- OMIMPS:311360 (MONDO:equivalentTo)
- Orphanet:95710 (MONDO:equivalentTo)
- ICD10CM:E28.3 (Orphanet:95710/ntbt)
Subsets
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders