Three M Syndrome 2; 3m2

Clinical Features

Top most frequent phenotypes and symptoms related to Three M Syndrome 2; 3m2

  • Short stature
  • Frontal bossing
  • Anteverted nares
  • Short neck
  • Long philtrum
  • Malar flattening
  • Midface retrusion
  • Hyperlordosis
  • Protruding ear
  • Dolichocephaly

And another 7 symptoms. If you need more information about this disease we can help you.

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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.

Alternative names

Three M Syndrome 2; 3m2 Is also known as 3m syndrome 2.

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.

Three M Syndrome 2; 3m2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
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 %
OBSL1. Complete sequencing.

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

OBSL1
Specificity
100 %
Genes
100 %
3-M syndrome 2 (sequence analysis of OBSL1 gene).

By CGC Genetics (Portugal).

OBSL1
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 %
Three M syndrome NGS panel.

By Connective Tissue Gene Tests (United States).

CUL7, CCDC8, OBSL1
Specificity
34 %
Genes
100 %
Three M syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests (United States).

CUL7, CCDC8, OBSL1
Specificity
34 %
Genes
100 %
Three M syndrome Comprehensive panel.

By Connective Tissue Gene Tests (United States).

CUL7, CCDC8, OBSL1
Specificity
34 %
Genes
100 %
Mental Retardation and Dysmorphology - panels.

By MGZ Medical Genetics Center (Germany).

RIT1, ROR2, RPL10, RPS6KA3, RRAS, SALL1, SF3B4, SGSH, ST3GAL3, SLC16A2, BRAF, SLC6A8, SLC9A6, SNAI2, SMARCA2, SMARCA4, SMARCB1, SMARCE1, ARID1A, SMC1A , (...)

View the complete list with 322 more genes
Specificity
1 %
Genes
100 %

You can get up to 26 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

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