FYCO1 gene related symptoms and diseases
All the information presented here about the FYCO1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to FYCO1 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Cataract | Very Common - Between 80% and 100% cases |
| Congenital cataract | Very Common - Between 80% and 100% cases |
| Sutural cataract | Uncommon - Between 30% and 50% cases |
| Lenticonus | Uncommon - Between 30% and 50% cases |
| Anterior polar cataract | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with FYCO1 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Cortical cataract
- Polar cataract
- Posterior polar cataract
- Inspiratory stridor
- Nuclear cataract
- Severe vision loss
- Preauricular pit
- Stridor
And 9 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to FYCO1 gene
Here you will find a list of rare diseases related to the FYCO1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CATARACT 18; CTRCT18
Alternate names
CATARACT 18; CTRCT18 Is also known as cataract, autosomal recessive congenital 2, catc2
Description
Mutations in the FYCO1 gene have been identified in families with autosomal recessive cataract described as congenital and congenital nuclear.The preferred title/symbol of this entry was formerly 'Cataract, Autosomal Recessive Congenital 2; CATC2.'
Most common symptoms of CATARACT 18; CTRCT18
- Cataract
- Congenital cataract
More info about CATARACT 18; CTRCT18
TOTAL EARLY-ONSET CATARACT
Alternate names
TOTAL EARLY-ONSET CATARACT Is also known as cataract, congenital, x-linked, cataract, congenital total, with posterior sutural opacities in heterozygotes, cxn, cct, cataract 40 with or without microcornea
Most common symptoms of TOTAL EARLY-ONSET CATARACT
- Cataract
- Visual impairment
- Ventricular septal defect
- Microphthalmia
- Patent ductus arteriosus
More info about TOTAL EARLY-ONSET CATARACT
Search interest in FYCO1
Potential gene panels for FYCO1 gene
MitoMet®Plus aCGH Analysis Panel
United States.
By Baylor Miraca Genetics Laboratories MitoMet®Plus aCGH Analysis that also includes the following genes: RGS9 RHO GRK1 RLBP1 RNASEL BCS1L RP1 RP2 RP9 RPE65
More info about this panel United States.
FYCO1. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the FYCO1 gene.
More info about this panel Spain.
Cataract 18, AR (sequence analysis of FYCO1 gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the FYCO1 gene.
More info about this panel Portugal.
Cataracts (NGS panel for 41 genes) Panel
Portugal.
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 panel Portugal.
Congenital Cataracts Sequencing Panel with CNV Detection Panel
United States.
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 panel United States.
Cataract Panel
Germany.
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 panel Germany.
Eye Diseases - panels Panel
Germany.
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 panel Germany.
Cataract panel Panel
Germany.
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 panel Germany.
Cataract, autosomal recessive congenital nuclear type 2 Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the FYCO1 gene.
More info about this panel Germany.
Cataract Panel Panel
Germany.
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 panel Germany.
Cataract Panel
Estonia.
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 panel Estonia.
Eye diseases comprehensive panel Panel
Estonia.
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 panel Estonia.
Invitae Congenital Cataracts Panel Panel
United States.
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 panel United States.
FYCO1 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the FYCO1 gene.
More info about this panel United States.
Cataract Panel Panel
Finland.
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 panel Finland.
Cataract 18, autosomal recessive Panel
Spain.
By Bioarray
This panel specifically test the FYCO1 gene.
More info about this panel Spain.
Congenital Cataract, Autosomal Recessive NGS and Deletion/Duplication Panel Panel
United States.
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children Congenital Cataract, Autosomal Recessive NGS and Deletion/Duplication Panel that also includes the following genes: FYCO1 AGK CRYAA CRYAB CRYBB1 CRYBB3 SIL1 CTDP1 TDRD7 GALK1
More info about this panel United States.
FYCO1 Gene Sequencing and Deletion/Duplication Analysis Panel
United States.
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
This panel specifically test the FYCO1 gene.
More info about this panel United States.
Autosomal Recessive Congenital Cataract Type 18 , Sequencing FYCO1 Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the FYCO1 gene.
More info about this panel Spain.
Congenital Cataracts , Panel Massive Sequencing (NGS) 40 Genes Panel
Spain.
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
More info about this panel Spain.
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ITPR1 BMPR1B