Cataract 36; Ctrct36
Clinical Features
Phenotypes and symptoms related to Cataract 36; Ctrct36
- 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.
Alternative names
Cataract 36; Ctrct36 Is also known as cataract, autosomal recessive congenital 4, catc4.
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 36; Ctrct36 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By CGC Genetics (Portugal).
TDRD7
Specificity
100 %
Genes
100 % |
![]() 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 % |
![]() By PreventionGenetics PreventionGenetics (United States).
BFSP1, BFSP2, VIM, FYCO1, PXDN, CHMP4B, P3H2, AGK, SLC16A12, CRYAA, CRYAB, CRYBA1, CRYBA4, CRYBB1, CRYBB2, CRYBB3, CRYGB, CRYGC, CRYGD, CRYGS , (...)
View the complete list with 20 more genes
Specificity
3 %
Genes
100 % |
![]() By MGZ Medical Genetics Center (Germany).
BFSP1, BFSP2, SIX6, VIM, WFS1, RAB18, FYCO1, JAM3, TBC1D20, CHMP4B, RAB3GAP1, RAB3GAP2, P3H2, VSX2, COL11A1, COL18A1, COL4A1, COL4A2, SLC16A12, CRYAA , (...)
View the complete list with 44 more genes
Specificity
2 %
Genes
100 % |
![]() 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 % |
![]() 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 % |
![]() By Centogene AG - the Rare Disease Company (Germany).
TDRD7
Specificity
100 %
Genes
100 % |
![]() 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 % |
You can get up to 7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like XERODERMA PIGMENTOSUM-COCKAYNE SYNDROME COMPLEX PSEUDOXANTHOMA ELASTICUM-LIKE SKIN MANIFESTATIONS WITH RETINITIS PIGMENTOSA CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie; CDG1E ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE; AMDH PREMATURE OVARIAN FAILURE 8; POF8 URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8