Cataract 44; Ctrct44
Table of contents:
Clinical Features
Phenotypes and symptoms related to Cataract 44; Ctrct44
- Cataract
- Visual loss
- 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.
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Cataract 44; Ctrct44 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 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 % |
 LSS.
By Fulgent Genetics Fulgent Genetics (United States).
LSS
Specificity
100 %
Genes
100 % |
Sources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; FPLD2 HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA; HTC3 GRACILE BONE DYSPLASIA; GCLEB WIEDEMANN-STEINER SYNDROME; WDSTS CONGENITAL MYOPATHY WITH MYASTHENIC-LIKE ONSET MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48; EIEE48
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