1. Mendelian
  2. Rare Diseases
  3. MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50

Mental Retardation, Autosomal Recessive 50; Mrt50

Table of contents:

Genes related to Mental Retardation, Autosomal Recessive 50; Mrt50

  • EDC3

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Mental Retardation, Autosomal Recessive 50; Mrt50

  • Intellectual disability
  • Hearing impairment
  • Microcephaly
  • Sensorineural hearing impairment
  • Intellectual disability, mild

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, Autosomal Recessive 50; Mrt50 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
EDC3.

By Fulgent Genetics Fulgent Genetics (United States).

EDC3
Specificity
100 %
Genes
100 %

You can get up to -7 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 PSORIASIS 14, PUSTULAR; PSORS14 COXOPODOPATELLAR SYNDROME COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3; COXPD3 MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K PERIPHERAL DYSOSTOSIS NIEMANN-PICK DISEASE, TYPE A