Mental Retardation, X-linked 101; Mrx101

Clinical Features

Top most frequent phenotypes and symptoms related to Mental Retardation, X-linked 101; Mrx101

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Strabismus
  • Abnormal facial shape
  • Absent speech
  • Hyperactivity
  • Macrotia
  • Protruding ear
  • Poor speech

And another 1 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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Mental Retardation, X-linked 101; Mrx101 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Non-Specific Intellectual Disability Panel.

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

RPS6KA3, CLIP1, SCN2A, ST3GAL3, SLC16A2, SLC25A1, SLC6A8, SLC9A6, SMARCA4, SMARCB1, ARID1A, SMC1A, KDM5C, SMS, SOX11, CDKL5, STXBP1, SYN1, SYNGAP1, SYP , (...)

View the complete list with 153 more genes
Specificity
1 %
Genes
100 %
Mental retardation, X-linked (NGS panel for 89 genes).

By CGC Genetics (Portugal).

RPS6KA3, SLC16A2, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, USP9X, ZNF711, ZNF81, FTSJ1, HDAC8 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
X-Linked Intellectual Disability Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RPL10, RPS6KA3, SLC16A2, SLC35A2, SLC6A8, SLC7A3, SLC9A6, SMC1A, KDM5C, SMS, SOX3, SSR4, CDKL5, SYN1, SYP, TAF1, TSPAN7, MED12, UBE2A, USP9X , (...)

View the complete list with 107 more genes
Specificity
1 %
Genes
100 %
Mental retardation - different panels.

By Institute of Human Genetics Uniklinik RWTH Aachen (Germany).

RGS7, RIT1, RMRP, BCS1L, RPL10, RPS6KA3, RRAS, SALL1, SC5D, ATXN10, BLM, SCN1A, SCN2A, SCN8A, SCO2, AIMP1, SDCCAG8, SDHA, SDHB, SGSH , (...)

View the complete list with 845 more genes
Specificity
1 %
Genes
100 %
Mental retardation, X-linked type 101.

By Centogene AG - the Rare Disease Company (Germany).

MID2
Specificity
100 %
Genes
100 %
qChip.

By Quantitative Genomic Medicine Laboratories, SL (Spain).

RS1, RUNX2, SALL1, SCN1A, BMPR1A, SH2D1A, SEM1, SHH, SHOX, SIM1, SIX3, SLC12A1, SLC12A3, FOXL2, BRAF, SMC1A, SNRPN, SOS1, SOX2, SOX3 , (...)

View the complete list with 105 more genes
Specificity
1 %
Genes
100 %
MID2.

By Fulgent Genetics Fulgent Genetics (United States).

MID2
Specificity
100 %
Genes
100 %

We have -1 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

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like CONE DYSTROPHY 3; COD3 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2 BETA-AMINOISOBUTYRIC ACIDURIA; BAIBA MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN IMINOGLYCINURIA LARON SYNDROME ACHONDROGENESIS TYPE 2

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