Mental Retardation, X-linked 103; Mrx103
Genes related to Mental Retardation, X-linked 103; Mrx103
Clinical FeaturesTop most frequent phenotypes and symptoms related to Mental Retardation, X-linked 103; Mrx103
- Intellectual disability
- Global developmental delay
- Anteverted nares
- Absent speech
- Coarse facial features
- Wide mouth
And another 2 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 researchersCurrently, 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 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
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
By Fulgent Genetics Fulgent Genetics (United States).
You can get up to -5 more panels with our dedicated toolLearn more
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 SEIZURES, BENIGN FAMILIAL INFANTILE, 5; BFIS5 DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3; DUH3 GUILLAIN-BARRE SYNDROME, FAMILIAL; GBS BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D LEIGH SYNDROME; LS