Meier-gorlin Syndrome 6; Mgors6

Clinical Features

Top most frequent phenotypes and symptoms related to Meier-gorlin Syndrome 6; Mgors6

  • Intellectual disability
  • Global developmental delay
  • Hearing impairment
  • Failure to thrive
  • Micrognathia
  • Strabismus
  • Cleft palate
  • Cryptorchidism
  • Feeding difficulties
  • Delayed speech and language development

And another 45 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

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 6; Mgors6 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Meier-Gorlin Syndrome Panel.

By Genetic Services Laboratory University of Chicago (United States).

ORC6, CDC6, GMNN, CDT1, ORC1, ORC4
Specificity
17 %
Genes
100 %
Comprehensive Primordial Dwarfism Panel.

By Genetic Services Laboratory University of Chicago (United States).

PLK4, XRCC4, CRIPT, PCNT, ORC6, CENPJ, CDC6, GMNN, RTTN, CDK5RAP2, CUL7, POC1A, CDT1, LARP7, CCDC8, SASS6, CEP63, OBSL1, CEP152, DNA2 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
100 %
Microcephalic primordial dwarfism Comprehensive panel.

By Connective Tissue Gene Tests (United States).

XRCC4, NIN, PCNT, ORC6, CENPJ, CDC45, CDC6, GMNN, CDT1, CEP63, CEP152, DNA2, DONSON, TRAIP, ATRIP, RNU4ATAC, LIG4, ORC1, ORC4, ATR , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %
Microcephalic primordial dwarfism Deletion / Duplication panel.

By Connective Tissue Gene Tests (United States).

XRCC4, NIN, PCNT, ORC6, CENPJ, CDC45, CDC6, GMNN, CDT1, CEP63, CEP152, DNA2, DONSON, TRAIP, ATRIP, RNU4ATAC, LIG4, ORC1, ORC4, ATR , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %
Meier-Gorlin syndrome NGS panel.

By Connective Tissue Gene Tests (United States).

ORC6, CDC45, CDC6, GMNN, CDT1, MCM5, ORC1, ORC4
Specificity
13 %
Genes
100 %
Microcephalic primordial dwarfism NGS panel.

By Connective Tissue Gene Tests (United States).

XRCC4, NIN, PCNT, ORC6, CENPJ, CDC45, CDC6, GMNN, CDT1, CEP63, CEP152, DNA2, DONSON, TRAIP, ATRIP, RNU4ATAC, LIG4, ORC1, ORC4, ATR , (...)

View the complete list with 1 more genes
Specificity
5 %
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 %

We have 2 more panels available in our App

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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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