Mental Retardation, X-linked 61; Mrx61

Clinical Features

Top most frequent phenotypes and symptoms related to Mental Retardation, X-linked 61; Mrx61

  • Intellectual disability
  • Global developmental delay
  • Microcephaly
  • Hypertelorism
  • Micrognathia
  • Cryptorchidism
  • Feeding difficulties
  • Wide nasal bridge
  • Behavioral abnormality
  • Broad forehead

And another 3 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

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.

Mental Retardation, X-linked 61; Mrx61 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 %
RLIM.

By Fulgent Genetics Fulgent Genetics (United States).

RLIM
Specificity
100 %
Genes
100 %

You can get up to -5 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6 CRANIOECTODERMAL DYSPLASIA 2; CED2 HEREDITARY ACROKERATOTIC POIKILODERMA, WEARY TYPE OHDO SYNDROME, SBBYS VARIANT; SBBYSS CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS; MDWH