Meier-gorlin Syndrome 7; Mgors7
Clinical Features
Top most frequent phenotypes and symptoms related to Meier-gorlin Syndrome 7; Mgors7
- Global developmental delay
- Short stature
- Hearing impairment
- Microcephaly
- Scoliosis
- Growth delay
- Strabismus
- Cleft palate
- Cryptorchidism
- High palate
And another 34 symptoms. If you need more information about this disease we can help you.
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.Meier-gorlin Syndrome 7; Mgors7 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Craniofacial Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
RUNX2, SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, ALX1, CD96, CDC45, WDR19, FAM20C, WDR35, IFT43, DPH1, EFNB1, MEGF8, ERF , (...)
View the complete list with 11 more genes
Specificity
4 %
Genes
100 % |
Craniofacial Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
RUNX2, SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, ALX1, CD96, CDC45, WDR19, FAM20C, WDR35, IFT43, DPH1, EFNB1, MEGF8, ERF , (...)
View the complete list with 11 more genes
Specificity
4 %
Genes
100 % |
Craniosynostosis.
By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center (United States).
RUNX2, SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, CDC45, ASXL1, WDR19, FREM1, WDR35, IFT43, EFNB1, MEGF8, ERF, FGFR1, FGFR2 , (...)
View the complete list with 7 more genes
Specificity
4 %
Genes
100 % |
Craniosynostosis Deletion / Duplication panel.
By Connective Tissue Gene Tests (United States).
SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, CDC45, WDR19, CYP26B1, SLC25A24, FREM1, WDR35, IFT43, EFNB1, MEGF8, ERF, FGFR1, FGFR2 , (...)
View the complete list with 6 more genes
Specificity
4 %
Genes
100 % |
Craniosynostosis Comprehensive panel.
By Connective Tissue Gene Tests (United States).
SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, CDC45, WDR19, CYP26B1, SLC25A24, FREM1, WDR35, IFT43, EFNB1, MEGF8, ERF, FGFR1, FGFR2 , (...)
View the complete list with 6 more genes
Specificity
4 %
Genes
100 % |
Craniosynostosis NGS panel.
By Connective Tissue Gene Tests (United States).
SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, CDC45, WDR19, CYP26B1, SLC25A24, FREM1, WDR35, IFT43, EFNB1, MEGF8, ERF, FGFR1, FGFR2 , (...)
View the complete list with 6 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 % |
You can get up to 12 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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