Cataract 45; Ctrct45

Clinical Features

Phenotypes and symptoms related to Cataract 45; Ctrct45

  • Cataract
  • Congenital cataract

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— The onset for some of the known clinical features related to this disease may vary, including congenital 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.

Cataract 45; Ctrct45 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Eye Diseases - panels.

By MGZ Medical Genetics Center (Germany).

BFSP1, BFSP2, SALL2, BMP4, BMP7, SHH, SIX3, SIX6, FOXL2, SOX2, TACSTD2, ZEB1, TFAP2A, TGFBI, TGIF1, TREX1, TYR, TYRP1, VAX1, VIM , (...)

View the complete list with 146 more genes
Specificity
1 %
Genes
100 %
Cataract panel.

By Centogene AG - the Rare Disease Company (Germany).

BFSP1, BFSP2, VIM, WFS1, UNC45B, FYCO1, CHMP4B, P3H2, VSX2, BCOR, LEMD2, AGK, SLC16A12, SIPA1L3, CRYAA, CRYAB, CRYBA1, CRYBA2, CRYBA4, CRYBB1 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
100 %
Cataract Panel.

By CeGaT GmbH (Germany).

BFSP1, BFSP2, VIM, FYCO1, PXDN, CHMP4B, P3H2, BCOR, AGK, SLC16A12, SIPA1L3, CRYAA, CRYAB, CRYBA1, CRYBA4, CRYBB1, CRYBB2, CRYBB3, CRYGA, CRYGB , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
100 %
Cataract.

By Asper Biogene Asper Biogene LLC (Estonia).

BFSP1, BFSP2, SIX6, VIM, UNC45B, FYCO1, PXDN, CHMP4B, P3H2, VSX2, BCOR, AGK, SLC16A12, SIPA1L3, CRYAA, CRYAB, CRYBA1, CRYBA4, CRYBB1, CRYBB2 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
100 %
SIPA1L3.

By Fulgent Genetics Fulgent Genetics (United States).

SIPA1L3
Specificity
100 %
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.

OMIM Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SCLEROSING CHOLANGITIS, NEONATAL; NSC TETRALOGY OF FALLOT; TOF IRON-REFRACTORY IRON DEFICIENCY ANEMIA; IRIDA DEAFNESS AND MYOPIA; DFNMYP COWDEN SYNDROME 1; CWS1 AMELOGENESIS IMPERFECTA, TYPE IJ; AI1J MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB