Meier-gorlin Syndrome 6; Mgors6

Clinical Features

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

  • Global developmental delay
  • Hearing impairment
  • Micrognathia
  • Strabismus
  • Failure to thrive
  • Motor delay
  • Cleft palate
  • Cryptorchidism
  • Depressed nasal bridge
  • Feeding difficulties
And another 44 symptoms. If you need more information about this disease we can help you.
Click here to know more about Mendelian.

Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

Accelerate your rare disease diagnosis with us

Learn more

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 in United States.

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

By Genetic Services Laboratory University of Chicago in United States.

CENPJ, CEP152, CDK5RAP2, PCNT, ATR, DNA2, TRIM37, RBBP8, LIG4, RTTN, CUL7, SASS6, CEP63, TRAIP, ORC1, GMNN, CDC6, CDT1, ORC6, ORC4 , (...)

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

By Connective Tissue Gene Tests in United States.

CENPJ, CEP152, PCNT, ATR, DNA2, RBBP8, LIG4, CEP63, TRAIP, NIN, CDC45, ORC1, GMNN, CDC6, CDT1, ORC6, ORC4, RNU4ATAC, XRCC4, ATRIP , (...)

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

By Connective Tissue Gene Tests in United States.

CENPJ, CEP152, PCNT, ATR, DNA2, RBBP8, LIG4, CEP63, TRAIP, NIN, CDC45, ORC1, GMNN, CDC6, CDT1, ORC6, ORC4, RNU4ATAC, XRCC4, ATRIP , (...)

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

By Connective Tissue Gene Tests in United States.

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

By Connective Tissue Gene Tests in United States.

CENPJ, CEP152, PCNT, ATR, DNA2, RBBP8, LIG4, CEP63, TRAIP, NIN, CDC45, ORC1, GMNN, CDC6, CDT1, ORC6, ORC4, RNU4ATAC, XRCC4, ATRIP , (...)

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

By Connective Tissue Gene Tests in United States.

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

By Connective Tissue Gene Tests in United States.

CDC45, ORC1, GMNN, CDC6, CDT1, ORC6, ORC4, MCM5
Specificity
13 %
Genes
100 %
Mental retardation - different panels.

By Institute of Human Genetics Cologne University in Germany.

FMR1, UBE3A, PTEN, MCCC1, MCCC2, ACAD9, PC, ANKH, HLCS, ATP7A, AUH, B4GALT7, BCKDHA, BCKDHB, BCS1L, C12orf65, ADSL, MMACHC, PRKCG, PAX6 , (...)

View the complete list with 847 more genes
Specificity
1 %
Genes
100 %
GMNN.

By Fulgent Genetics Fulgent Genetics in United States.

GMNN
Specificity
100 %
Genes
100 %


Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more

Other rare diseases that you may find interesting

REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET; RBMX1B PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY; PDHXD PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH BARDET-BIEDL SYNDROME 1; BBS1 ANTIPHOSPHOLIPID SYNDROME, FAMILIAL ANTERIOR SEGMENT DYSGENESIS 1; ASGD1 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H