Mental Retardation, X-linked 103; Mrx103

Clinical Features

Top most frequent phenotypes and symptoms related to Mental Retardation, X-linked 103; Mrx103

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Cryptorchidism
  • Ventriculomegaly
  • Anteverted nares
  • Absent speech
  • Micropenis
  • Coarse facial features
  • Wide mouth

And another 2 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 103; Mrx103 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
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 %
KLHL15.

By Fulgent Genetics Fulgent Genetics (United States).

KLHL15
Specificity
100 %
Genes
100 %

We have -5 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

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM; HLD8 OVARIAN HYPERSTIMULATION SYNDROME; OHSS HYPERCHLORHIDROSIS, ISOLATED HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1; FPH1 D-2-HYDROXYGLUTARIC ACIDURIA 1; D2HGA1 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49 AUTOSOMAL RECESSIVE ATAXIA DUE TO PEX10 DEFICIENCY

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