Premature Ovarian Failure 2a; Pof2a

Clinical Features

Phenotypes and symptoms related to Premature Ovarian Failure 2a; Pof2a

  • Premature ovarian insufficiency
  • Secondary amenorrhea

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Premature Ovarian Failure 2a; Pof2a Recommended genes panels

Panel Name, Specifity and genes Tested/covered
DIAPH2.

By Fulgent Genetics Fulgent Genetics (United States).

DIAPH2
Specificity
100 %
Genes
100 %
PRIMARY OVARIAN FAILURE.

By Laboratorio de Genetica Clinica SL (Spain).

BMP15, FOXL2, DIAPH2, FSHR
Specificity
25 %
Genes
100 %
Premature Ovarian Failure (POF) and Related Disorders , Panel Massive Sequencing (NGS) 14 Genes.

By Reference Laboratory Genetics (Spain).

BMP15, FOXL2, STAR, WNT4, POF1B, PSMC3IP, NOBOX, FIGLA, CYP17A1, CYP19A1, DIAPH2, FSHB, FSHR, NR5A1
Specificity
8 %
Genes
100 %
Tempus xO assay.

By Tempus Labs, Inc. (United States).

BCL6, RHEB, RIPK1, RIPK2, RIPK3, RIT1, BCL7A, BCL9, BCR, ROBO2, ROCK1, ROCK2, ROR1, ROR2, ROS1, RPA1, BDNF, RPL5, RPN1, RPS6KB1 , (...)

View the complete list with 1627 more genes
Specificity
1 %
Genes
100 %
Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis.

By CEN4GEN Institute for Genomics and Molecular Diagnostics (Canada).

BMP15, FOXL2, POF1B, PSMC3IP, HFM1, NOBOX, FIGLA, CYP17A1, CYP19A1, DIAPH2, EIF2B2, EIF2B3, EIF2B5, FMR1, FSHR, GALT, GDF9, LHCGR, LMNA, NR5A1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %

You can get up to -3 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like WOLMAN DISEASE PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II; PMDS HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1 DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1 CAMURATI-ENGELMANN DISEASE; CAEND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1; PNH1 EBSTEIN ANOMALY