HNMT gene related symptoms and diseases
All the information presented here about the HNMT gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to HNMT gene
Symptoms // Phenotype | % Cases |
---|---|
Fever | Uncommon - Between 30% and 50% cases |
Chest tightness | Uncommon - Between 30% and 50% cases |
Intellectual disability, severe | Uncommon - Between 30% and 50% cases |
Motor delay | Uncommon - Between 30% and 50% cases |
Delayed speech and language development | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with HNMT gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Microcephaly
- Global developmental delay
- Intellectual disability
- Allergic rhinitis
- Respiratory distress
- Atopic dermatitis
- Wheezing
- Inflammatory abnormality of the skin
And 5 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to HNMT gene
Here you will find a list of rare diseases related to the HNMT. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ASTHMA, SUSCEPTIBILITY TO
Alternate names
ASTHMA, SUSCEPTIBILITY TO Is also known as asthma, bronchial, asthma-related traits, susceptibility to
Description
Bronchial asthma is the most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment.Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002; Pillai et al., 2006). See {147050} for information on the asthma-associated phenotype atopy.
Most common symptoms of ASTHMA, SUSCEPTIBILITY TO
- Fever
- Respiratory distress
- Dyspnea
- Cough
- Asthma
More info about ASTHMA, SUSCEPTIBILITY TO
SOURCES: OMIM
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51; MRT51
Most common symptoms of MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51; MRT51
- Intellectual disability
- Global developmental delay
- Microcephaly
- Delayed speech and language development
- Motor delay
More info about MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51; MRT51
SOURCES: OMIM
AUTOSOMAL RECESSIVE NON-SYNDROMIC INTELLECTUAL DISABILITY
Alternate names
AUTOSOMAL RECESSIVE NON-SYNDROMIC INTELLECTUAL DISABILITY Is also known as ar-nsid, ns-arid
More info about AUTOSOMAL RECESSIVE NON-SYNDROMIC INTELLECTUAL DISABILITY
SOURCES: ORPHANET
Search interest in HNMT
Potential gene panels for HNMT gene
Test for Asthma, Susceptibility to Panel
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
This panel specifically test the HNMT gene.
More info about this panelHistamine intolerance Panel
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Histamine intolerance that also includes the following genes: HNMT AOC1
More info about this panelAsthma, susceptibility to Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the HNMT gene.
More info about this panelAsthma, susceptibility to Panel
By MedGene
This panel specifically test the HNMT gene.
More info about this panelHNMT Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the HNMT gene.
More info about this panelAsthma Susceptibility to, Panel Massive Sequencing (NGS) 10 Genes Panel
By Reference Laboratory Genetics Asthma Susceptibility to, Panel Massive Sequencing (NGS) 10 Genes that also includes the following genes: CCL11 TNF SCGB3A2 ALOX5 HLA-G HNMT IL13 MUC7 PLA2G7
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