Meier-gorlin Syndrome 3; Mgors3

Clinical Features

Top most frequent phenotypes and symptoms related to Meier-gorlin Syndrome 3; Mgors3

  • Short stature
  • Microcephaly
  • Growth delay
  • Failure to thrive
  • Micrognathia
  • Cryptorchidism
  • Low-set ears
  • Feeding difficulties
  • Delayed speech and language development
  • Motor delay

And another 41 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 3; Mgors3 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 %
Microcephaly Sequencing Panel.

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

STIL, SLC2A1, SLC9A6, PLK4, CDKL5, TCF4, UBE3A, WWOX, RAB18, CRIPT, SLC25A19, ZEB2, CASK, TSEN34, ZNF335, ARFGEF2, PCNT, TBC1D20, TUBGCP4, STAMBP , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
100 %
Microcephaly Deletion/Duplication Panel.

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

STIL, SLC1A4, SLC2A1, SLC9A6, SOX11, PLK4, CDKL5, TCF4, UBE3A, USP18, WWOX, RAB18, CRIPT, SLC25A19, ZEB2, NIN, PPP1R15B, CASK, TSEN34, ZNF335 , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
100 %
Meier-Gorlin Syndrome 3.

By Molecular Diagnostics Lab Nemours Alfred I. duPont Hospital for Children (United States).

ORC6
Specificity
100 %
Genes
100 %
Meier-Gorlin Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

ORC6, CDC6, CDT1, ORC1, ORC4
Specificity
20 %
Genes
100 %
Meier-Gorlin Syndrome via ORC6 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

ORC6
Specificity
100 %
Genes
100 %
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RMRP, ROR2, RUNX2, SALL1, BMP1, BMP2, BMPR1B, SF3B4, SH3BP2, FBXW4, SHH, SHOX, SKI, SLCO2A1, SLC26A2, SMARCAL1, SMC1A, SOX9, SQSTM1, TBX15 , (...)

View the complete list with 236 more genes
Specificity
1 %
Genes
100 %

We have 22 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

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