Corneal Dystrophy, Lattice Type Iiia; Cdl3a

Clinical Features

Phenotypes and symptoms related to Corneal Dystrophy, Lattice Type Iiia; Cdl3a

  • Pain
  • Visual impairment
  • Reduced visual acuity
  • Corneal dystrophy
  • Corneal erosion
  • Lattice corneal dystrophy

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

Corneal Dystrophy, Lattice Type Iiia; Cdl3a Is also known as lattice corneal dystrophy, type iiia.

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.

Corneal Dystrophy, Lattice Type Iiia; Cdl3a Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMetĀ®Plus aCGH Analysis.

By Baylor Miraca Genetics Laboratories (United States).

RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB , (...)

View the complete list with 612 more genes
Specificity
1 %
Genes
100 %
TGFBI.

By Institute for Human Genetics University Clinic Freiburg (Germany).

TGFBI
Specificity
100 %
Genes
100 %
TGFBI. Detection of the mutations in 124 and 555 codons by sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

TGFBI
Specificity
100 %
Genes
100 %
TGFBI. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

TGFBI
Specificity
100 %
Genes
100 %
Corneal dystrophy, Avellino type (mutations pArg555trp and pArg124His on TGFBI gene).

By CGC Genetics (Portugal).

TGFBI
Specificity
100 %
Genes
100 %
Hereditary amyloidosis (NGS panel of 19 genes).

By CGC Genetics (Portugal).

TACSTD2, TGFBI, TNFRSF1A, TTR, NLRP3, IL31RA, CST3, F10, FGA, GSN, APP, LYZ, MEFV, OSMR, B2M, PRNP, RET
Specificity
6 %
Genes
100 %
Hereditary amyloidosis (NGS panel of 19 genes).

By CGC Genetics (Portugal).

TACSTD2, TGFBI, TNFRSF1A, TTR, NLRP3, IL31RA, CST3, F10, FGA, GSN, APP, LYZ, MEFV, OSMR, B2M, PRNP, RET
Specificity
6 %
Genes
100 %
Corneal dystrophy, TGFBI gene mutation analysis.

By Laboratory of Genetics BioTe21 Adam Master (Poland).

TGFBI
Specificity
100 %
Genes
100 %

You can get up to 17 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

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