Mental Retardation, Autosomal Recessive 51; Mrt51

Clinical Features

Phenotypes and symptoms related to Mental Retardation, Autosomal Recessive 51; Mrt51

  • Intellectual disability
  • Global developmental delay
  • Microcephaly
  • Delayed speech and language development
  • Motor delay
  • Intellectual disability, severe
  • Poor speech

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 51; Mrt51 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Test for Asthma, Susceptibility to.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders (Germany).

HNMT
Specificity
100 %
Genes
100 %
Histamine intolerance.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders (Germany).

HNMT, AOC1
Specificity
50 %
Genes
100 %
Asthma, susceptibility to.

By Praxis fuer Humangenetik Wien (Austria).

HNMT
Specificity
100 %
Genes
100 %
Asthma, susceptibility to.

By MedGene (Slovakia).

HNMT
Specificity
100 %
Genes
100 %
HNMT.

By Fulgent Genetics Fulgent Genetics (United States).

HNMT
Specificity
100 %
Genes
100 %
Asthma Susceptibility to, Panel Massive Sequencing (NGS) 10 Genes.

By Reference Laboratory Genetics (Spain).

CCL11, TNF, SCGB3A2, ALOX5, HLA-G, HNMT, IL13, MUC7, PLA2G7
Specificity
12 %
Genes
100 %

You can get up to -2 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 SEVERE CUTANEOUS ADVERSE REACTION, SUSCEPTIBILITY TO PEELING SKIN SYNDROME 5; PSS5 DEAFNESS, AUTOSOMAL RECESSIVE 93; DFNB93 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD LEUKODYSTROPHY, HYPOMYELINATING, 12; HLD12 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10; COXPD10 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32