Mental Retardation, Autosomal Recessive 51; Mrt51

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Mental Retardation, Autosomal Recessive 51; Mrt51

HNMT

View recommended genes panels

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 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA PERRAULT SYNDROME 3; PRLTS3 DYSTONIA 11, MYOCLONIC; DYT11 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie; CDG1E CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1; CDCBM1 CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1 LONG QT SYNDROME 9; LQT9