premature ovarian failure 1

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Disease Overview

Any primary ovarian failure in which the cause of the disease is a mutation in the FMR1 gene.

Synonyms

FMR1 primary ovarian failure
FMR1-related premature ovarian failure
FMR1-related primary ovarian insufficiency
Pof1
familial premature ovarian failure
fragile X-associated primary ovarian insufficiency
fragile x-associated primary ovarian insufficiency
hypergonadotropic ovarian failure, X-linked
idiopathic familial premature ovarian failure
ovarian failure, premature
premature ovarian failure 1
premature ovarian failure type 1
premature ovarian failure, X-linked
primary ovarian failure caused by mutation in FMR1

Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.