Leber Congenital Amaurosis 16; Lca16

Clinical Features

Top most frequent phenotypes and symptoms related to Leber Congenital Amaurosis 16; Lca16

  • Nystagmus
  • Strabismus
  • Cataract
  • Visual impairment
  • Rod-cone dystrophy
  • Reduced visual acuity
  • Photophobia
  • Pallor
  • Nyctalopia
  • Retinal dystrophy

And another 6 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

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.

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.

Leber Congenital Amaurosis 16; Lca16 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMet®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 %
KCNJ13 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KCNJ13
Specificity
100 %
Genes
100 %
KCNJ13 Familial Mutation/Variant Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KCNJ13
Specificity
100 %
Genes
100 %
KCNJ13 Prenatal Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KCNJ13
Specificity
100 %
Genes
100 %
KCNJ13 Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KCNJ13
Specificity
100 %
Genes
100 %
KCNJ13 Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KCNJ13
Specificity
100 %
Genes
100 %
Leber Congential Amaurosis Panel (MitomeNGS).

By Baylor Miraca Genetics Laboratories (United States).

RPE65, TULP1, RPGRIP1, CABP4, NMNAT1, RD3, RDH12, SPATA7, CRB1, CRX, IQCB1, CEP290, LCA5, AIPL1, GUCY2D, IMPDH1, KCNJ13, LRAT, OTX2
Specificity
6 %
Genes
100 %
Leber Congenital Amaurosis Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

RPE65, TULP1, RPGRIP1, CABP4, NMNAT1, CLUAP1, RD3, RDH12, SPATA7, CRB1, CRX, IQCB1, CEP290, IFT140, LCA5, AIPL1, DTHD1, GDF6, GUCY2D, IMPDH1 , (...)

View the complete list with 4 more genes
Specificity
5 %
Genes
100 %

You can get up to 42 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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