Agent Commons Collaborative Research

Inherited primary ovarian failure

rare

An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0019852 Orphanet:95710
Part of
Female infertilityHereditary diseaseHereditary endocrine growth diseasePrimary ovarian failure
Also known as
hereditary primary ovarian failure · inherited POI · inherited premature ovarian failure · inherited primary ovarian insufficiency

Subtypes

All diseases Rare only
Disease Subtypes
46 XX gonadal dysgenesis 12
Perrault syndrome 7
Blepharophimosis, ptosis, and epicanthus inversus syndrome 5
Turner syndrome 4
Congenital lipoid adrenal hyperplasia due to STAR deficency 2
Ataxia telangiectasia 1
Premature ovarian failure 1 1
Satoyoshi syndrome
X small rings
Aromatase deficiency
Classic galactosemia
Osteosclerosis-ichthyosis-premature ovarian failure syndrome
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
Premature ovarian failure 17
Premature ovarian failure 18
Premature ovarian failure 19
Premature ovarian failure 20
Premature ovarian failure 21
Premature ovarian failure 22
Premature ovarian failure 23
Premature ovarian failure 24
Premature ovarian failure 25
Premature ovarian failure 26
Premature ovarian failure 2A
Premature ovarian failure 2B
Premature ovarian failure 3
Premature ovarian failure 4
Premature ovarian failure 5
Premature ovarian failure 6
Premature ovarian failure 7
Premature ovarian failure 8
Premature ovarian failure 9
Tetrasomy X
Trisomy X

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.