Cataract 43; Ctrct43
Table of contents:
Clinical Features
Phenotypes and symptoms related to Cataract 43; Ctrct43
- Cataract
- Subcapsular 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 43; Ctrct43 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 type 43.
By Centogene AG - the Rare Disease Company (Germany).
UNC45B
Specificity
100 %
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 % |
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 Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT HEPATIC DISEASE; PKD4 HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME FARBER LIPOGRANULOMATOSIS; FRBRL LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2