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Premature ovarian failure 10

Summary

Premature ovarian failure-10 (POF10) represents a syndrome characterized by primary amenorrhea, hypergonadotropic ovarian insufficiency, and genomic instability in somatic cells. For a general phenotypic description and discussion of genetic heterogeneity of premature ovarian failure, see POF1 (311360). For a discussion of genetic heterogeneity of age at natural menopause, see MENOQ1 (300488). [from OMIM]

Available tests

6 tests are in the database for this condition.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C20orf154, POF10, dJ967N21.5, MCM8
    Summary: minichromosome maintenance 8 homologous recombination repair factor

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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