MIR184 gene related symptoms and diseases

All the information presented here about the MIR184 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to MIR184 gene

Symptoms // Phenotype % Cases
Cataract Very Common - Between 80% and 100% cases
Myopia Very Common - Between 80% and 100% cases
Reduced visual acuity Very Common - Between 80% and 100% cases
Corneal opacity Very Common - Between 80% and 100% cases
Congenital cataract Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with MIR184 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Astigmatism
  • Microcornea
  • Ectropion
  • Keratoconus
  • Hypoplasia of the iris
  • Ectopia pupillae
  • Anterior segment developmental abnormality
  • Abnormal cornea morphology

And 3 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to MIR184 gene

Here you will find a list of rare diseases related to the MIR184. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


EDICT SYNDROME

Alternate names

EDICT SYNDROME Is also known as endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome, familial keratoconus with cataract, keratoconus, familial, with early-onset anterior polar cataract, endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal

Description

EDICT (endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning) syndrome is a very rare eye disorder representing a constellation of autosomal dominantly inherited ocular findings, including early-onset or congenital cataracts, corneal stromal thinning, early-onset keratoconus, corneal endothelial dystrophy, and iris hypoplasia.

Most common symptoms of EDICT SYNDROME

  • Cataract
  • Myopia
  • Reduced visual acuity
  • Corneal opacity
  • Congenital cataract


More info about EDICT SYNDROME

SOURCES: OMIM ORPHANET


Potential gene panels for MIR184 gene

Ocular anterior segment mesenchymal dysgenesis (NGS panel of 18 genes) Panel

Portugal.

By CGC Genetics Ocular anterior segment mesenchymal dysgenesis (NGS panel of 18 genes) that also includes the following genes: BMP4 VSX1 PXDN B3GLCT COL4A1 CYP1B1 MIR184 SLC38A8 FGFR2 FOXC1

More info about this panel
Portugal.

Ocular anterior segment mesenchymal dysgenesis (NGS panel of 18 genes) Panel

Portugal.

By CGC Genetics Ocular anterior segment mesenchymal dysgenesis (NGS panel of 18 genes) that also includes the following genes: BMP4 VSX1 PXDN B3GLCT COL4A1 CYP1B1 MIR184 SLC38A8 FGFR2 FOXC1

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.

Keratoconus and related disorders Comprehensive test Panel

United States.

By Connective Tissue Gene Tests Keratoconus and related disorders Comprehensive test that also includes the following genes: VSX1 ZNF469 MIR184 PRDM5

More info about this panel
United States.

Keratoconus and related disorders Deletion / Duplication test Panel

United States.

By Connective Tissue Gene Tests Keratoconus and related disorders Deletion / Duplication test that also includes the following genes: VSX1 ZNF469 MIR184 PRDM5

More info about this panel
United States.

Keratoconus and related disorders NGS test Panel

United States.

By Connective Tissue Gene Tests Keratoconus and related disorders NGS test that also includes the following genes: VSX1 ZNF469 MIR184 PRDM5

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.

Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome Panel

Germany.

By MGZ Medical Genetics Center Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome that also includes the following genes: B3GLCT COL4A1 COL4A2 CYP1B1 MIR184 SLC38A8 EYA1 FOXC1 FOXE3 LTBP2

More info about this panel
Germany.

MIR184 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the MIR184 gene.

More info about this panel
United States.

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.

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