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inherited primary ovarian failure

Go to external page http://purl.obolibrary.org/obo/MONDO_0019852

An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: inherited POI hereditary primary ovarian failure inherited premature ovarian failure inherited primary ovarian insufficiency

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:95710 (MONDO:equivalentTo)
  • ICD10CM:E28.3 (Orphanet:95710/ntbt)
  • GARD:19294 (MONDO:GARD)
  • OMIMPS:311360 (MONDO:equivalentTo)
  • UMLS:C2930861 (MONDO:equivalentTo)
  • MEDGEN:443920 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/6877

exactMatch

http://www.orpha.net/ORDO/Orphanet_95710

http://identifiers.org/medgen/443920

https://omim.org/phenotypicSeries/PS311360

http://linkedlifedata.com/resource/umls/id/C2930861

has related synonym

non-acquired premature ovarian failure

id

MONDO:0019852