1. Mendelian
  2. Genes
  3. HMGB1

HMGB1 gene related symptoms and diseases

All the information presented here about the HMGB1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to HMGB1 gene

Symptoms // Phenotype % Cases
Peripheral neuropathy Very Common - Between 80% and 100% cases
Fever Very Common - Between 80% and 100% cases
Skeletal muscle atrophy Very Common - Between 80% and 100% cases
Lower limb muscle weakness Very Common - Between 80% and 100% cases

Rare diseases associated to HMGB1 gene

Here you will find a list of rare diseases related to the HMGB1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


NEUROPATHY, PAINFUL

Most common symptoms of NEUROPATHY, PAINFUL

  • Peripheral neuropathy
  • Fever
  • Skeletal muscle atrophy
  • Lower limb muscle weakness


More info about NEUROPATHY, PAINFUL

SOURCES: OMIM MESH


Potential gene panels for HMGB1 gene

HMGB1 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the HMGB1 gene.

More info about this panel
United States.

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