CRYGS gene related symptoms and diseases
All the information presented here about the CRYGS gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CRYGS gene
Symptoms // Phenotype | % Cases |
---|---|
Cataract | Very Common - Between 80% and 100% cases |
Cortical cataract | Uncommon - Between 30% and 50% cases |
Membranous cataract | Uncommon - Between 30% and 50% cases |
Congenital cataract | Uncommon - Between 30% and 50% cases |
Rare diseases associated to CRYGS gene
Here you will find a list of rare diseases related to the CRYGS. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CATARACT 20, MULTIPLE TYPES; CTRCT20
Description
Mutation in the CRYGS gene has been identified in multiple types of cataract, which have been described as progressive polymorphic anterior, posterior, or peripheral cortical.
Most common symptoms of CATARACT 20, MULTIPLE TYPES; CTRCT20
- Cataract
- Cortical cataract
- Membranous cataract
More info about CATARACT 20, MULTIPLE TYPES; CTRCT20
SOURCES: OMIM
CATARACT 25; CTRCT25
Alternate names
CATARACT 25; CTRCT25 Is also known as ccsso, cataract, central pouch-like, with sutural opacities, cataract, central saccular, with sutural opacities
Most common symptoms of CATARACT 25; CTRCT25
- Cataract
- Congenital cataract
More info about CATARACT 25; CTRCT25
Search interest in CRYGS
Potential gene panels for CRYGS gene
Cataracts (NGS panel for 41 genes) Panel
By CGC Genetics Cataracts (NGS panel for 41 genes) that also includes the following genes: BFSP1 BFSP2 VIM WFS1 FYCO1 PXDN CHMP4B P3H2 AGK SLC16A12
More info about this panelCongenital Cataracts Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Congenital Cataracts Sequencing Panel with CNV Detection that also includes the following genes: BFSP1 BFSP2 VIM FYCO1 PXDN CHMP4B P3H2 AGK SLC16A12 CRYAA
More info about this panelCataract Panel
By MGZ Medical Genetics Center Cataract that also includes the following genes: BFSP1 BFSP2 SIX6 VIM WFS1 RAB18 FYCO1 JAM3 TBC1D20 CHMP4B
More info about this panelEye Diseases - panels Panel
By MGZ Medical Genetics Center Eye Diseases - panels that also includes the following genes: BFSP1 BFSP2 SALL2 BMP4 BMP7 SHH SIX3 SIX6 FOXL2 SOX2
More info about this panelCataract panel Panel
By Centogene AG - the Rare Disease Company Cataract panel that also includes the following genes: BFSP1 BFSP2 VIM WFS1 UNC45B FYCO1 CHMP4B P3H2 VSX2 BCOR
More info about this panelCataract Panel Panel
By CeGaT GmbH Cataract Panel that also includes the following genes: BFSP1 BFSP2 VIM FYCO1 PXDN CHMP4B P3H2 BCOR AGK SLC16A12
More info about this panelCataract Panel
By Asper Biogene Asper Biogene LLC Cataract that also includes the following genes: BFSP1 BFSP2 SIX6 VIM UNC45B FYCO1 PXDN CHMP4B P3H2 VSX2
More info about this panelEye diseases comprehensive panel Panel
By Asper Biogene Asper Biogene LLC Eye diseases comprehensive panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelInvitae Congenital Cataracts Panel Panel
By Invitae Invitae Congenital Cataracts Panel that also includes the following genes: BFSP1 BFSP2 FYCO1 VSX2 BCOR AGK CRYAA CRYAB CRYBA1 CRYBB1
More info about this panelCRYGS Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CRYGS gene.
More info about this panelCataract Panel Panel
By Blueprint Genetics Cataract Panel that also includes the following genes: BFSP1 BFSP2 TFAP2A VIM WFS1 WRN FYCO1 PXDN CHMP4B RAB3GAP1
More info about this panelCongenital Cataracts , Panel Massive Sequencing (NGS) 40 Genes Panel
By Reference Laboratory Genetics Congenital Cataracts , Panel Massive Sequencing (NGS) 40 Genes that also includes the following genes: BFSP1 BFSP2 VIM FYCO1 PXDN CHMP4B P3H2 AGK SLC16A12 CRYAA
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