Mental Retardation, Autosomal Recessive 51; Mrt51
Genes related to Mental Retardation, Autosomal Recessive 51; Mrt51
- HNMT
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 moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PSORIASIS 1, SUSCEPTIBILITY TO; PSORS1 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR CRANIODIAPHYSEAL DYSPLASIA; CDD CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1; CDCBM1 VAN MALDERGEM SYNDROME 1; VMLDS1 AMELOGENESIS IMPERFECTA, TYPE IG; AI1G