Meier-gorlin Syndrome 8; Mgors8

Clinical Features

Phenotypes and symptoms related to Meier-gorlin Syndrome 8; Mgors8

  • Micrognathia
  • Cryptorchidism
  • Ptosis
  • Low-set ears
  • Narrow mouth
  • Microtia
  • Thick vermilion border
  • Renal hypoplasia
  • Bilateral cryptorchidism

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.


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Meier-gorlin Syndrome 8; Mgors8 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Meier-Gorlin syndrome NGS panel.

By Connective Tissue Gene Tests (United States).

ORC6, CDC45, CDC6, GMNN, CDT1, MCM5, ORC1, ORC4
Specificity
13 %
Genes
100 %
Meier-Gorlin syndrome Comprehensive panel.

By Connective Tissue Gene Tests (United States).

ORC6, CDC45, CDC6, GMNN, CDT1, MCM5, ORC1, ORC4
Specificity
13 %
Genes
100 %
Meier-Gorlin syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests (United States).

ORC6, CDC45, CDC6, GMNN, CDT1, MCM5, ORC1, ORC4
Specificity
13 %
Genes
100 %
MCM5.

By Fulgent Genetics Fulgent Genetics (United States).

MCM5
Specificity
100 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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