Term info
database cross reference
- OMIMPS:311360 (MONDO:equivalentTo)
- ICD10CM:E28.3 (Orphanet:95710/ntbt)
- Orphanet:95710 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome.
exactMatch
https://omim.org/phenotypicSeries/PS311360, http://purl.obolibrary.org/obo/Orphanet_95710
has exact synonym
hereditary primary ovarian failure, inherited premature ovarian failure
has related synonym
non-acquired premature ovarian failure
id
MONDO:0019852