General Information of Disease (ID: DIS4V9SY)

Disease Name Inherited primary ovarian failure
Synonyms non-acquired premature ovarian failure; inherited premature ovarian failure; hereditary primary ovarian failure
Definition An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome.
Disease Hierarchy
DISYKSRF: Genetic disease
DIS19L71: Pediatric growth disorder
DISWASB4: Female hypogonadism
DIS4V9SY: Inherited primary ovarian failure
Disease Identifiers
MONDO ID
MONDO_0019852
MESH ID
C535272
UMLS CUI
C2930861
MedGen ID
443920
Orphanet ID
95710