Cataract 42; Ctrct42
Table of contents:
Clinical Features
Phenotypes and symptoms related to Cataract 42; Ctrct42
- Cataract
- Myopia
- Glaucoma
- 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.)— 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.Cataract 42; Ctrct42 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Cataracts (NGS panel for 41 genes).
By CGC Genetics (Portugal).
BFSP1, BFSP2, VIM, WFS1, FYCO1, PXDN, CHMP4B, P3H2, AGK, SLC16A12, CRYAA, CRYAB, CRYBA1, CRYBA2, CRYBA4, CRYBB1, CRYBB2, CRYBB3, CRYGB, CRYGC , (...)
View the complete list with 21 more genes
Specificity
3 %
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 % |
 CRYBA2.
By Fulgent Genetics Fulgent Genetics (United States).
CRYBA2
Specificity
100 %
Genes
100 % |
You can get up to -5 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like WAARDENBURG SYNDROME, TYPE 4C; WS4C JOUBERT SYNDROME 23; JBTS23 GLYCEROL KINASE DEFICIENCY; GKD EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1 BLAU SYNDROME; BLAUS NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A MENTAL RETARDATION, X-LINKED 61; MRX61