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


Potential gene panels for HNMT gene

Test for Asthma, Susceptibility to Panel

Germany.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders

This panel specifically test the HNMT gene.

More info about this panel
Germany.

Histamine intolerance Panel

Germany.

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 panel
Germany.

Asthma, susceptibility to Panel

Austria.

By Praxis fuer Humangenetik Wien

This panel specifically test the HNMT gene.

More info about this panel
Austria.

Asthma, susceptibility to Panel

Slovakia.

By MedGene

This panel specifically test the HNMT gene.

More info about this panel
Slovakia.

HNMT Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the HNMT gene.

More info about this panel
United States.

Asthma Susceptibility to, Panel Massive Sequencing (NGS) 10 Genes Panel

Spain.

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

More info about this panel
Spain.

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ARMS2 CCNF PYROXD1 CYP3A5