Macular Degeneration, Age-related, 11; Armd11

Clinical Features

Phenotypes and symptoms related to Macular Degeneration, Age-related, 11; Armd11

  • Macular degeneration

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— The onset for some of the known clinical features related to this disease may vary, including late 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.

Macular Degeneration, Age-related, 11; Armd11 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
CST3. Complete sequencing.

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

CST3
Specificity
100 %
Genes
100 %
Cerebral amyloid angiopathy (sequence analysis of CST3 gene).

By CGC Genetics (Portugal).

CST3
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 %
Vascular and connective tissue diseases - panels.

By MGZ Medical Genetics Center (Germany).

AIMP1, BMPR1B, BMPR2, SKI, TGFB2, TGFB3, TGFBR1, TGFBR2, TNXB, TREX1, TTR, ACTA2, SLC2A10, CACNA1C, CAV1, CBS, JAM3, COQ8A, ACVRL1, ADA2 , (...)

View the complete list with 46 more genes
Specificity
2 %
Genes
100 %
Macular degeneration, age-related type 11.

By Centogene AG - the Rare Disease Company (Germany).

CST3
Specificity
100 %
Genes
100 %
Cerebral amyloid angiopathy.

By Centogene AG - the Rare Disease Company (Germany).

CST3
Specificity
100 %
Genes
100 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company (Germany).

BCS1L, ROR2, RPL10, BDNF, RPS6KA3, RTN2, RYR1, SACS, BIN1, SBF1, SCN10A, SCN1A, SCN1B, SCN2A, SCN3A, SCN4A, SCN5A, SCN8A, SCN9A, SCO1 , (...)

View the complete list with 1177 more genes
Specificity
1 %
Genes
100 %

You can get up to 6 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

MESH OMIM Genetic Syndrome Finder

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