HMOX1 gene related symptoms and diseases

All the information presented here about the HMOX1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to HMOX1 gene

Symptoms // Phenotype % Cases
Asthma Uncommon - Between 30% and 50% cases
Abnormal lung morphology Uncommon - Between 30% and 50% cases
Emphysema Uncommon - Between 30% and 50% cases
Bronchitis Uncommon - Between 30% and 50% cases
Chronic lung disease Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with HMOX1 gene alterations may also develop some of the following symptoms and phenotypes:
  • Not very common - Between 30% and 50% cases

  • Chronic obstructive pulmonary disease
  • Chronic bronchitis
  • Growth delay
  • Anemia
  • Hepatomegaly
  • Fever
  • Proteinuria
  • Skin rash

And 3 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to HMOX1 gene

Here you will find a list of rare diseases related to the HMOX1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


PULMONARY DISEASE, CHRONIC OBSTRUCTIVE; COPD


Description

Chronic obstructive pulmonary disease (COPD) is a common, complex disorder associated with substantial morbidity and mortality. COPD is defined by irreversible airflow obstruction due to chronic bronchitis, emphysema, and/or small airways disease. Airflow obstruction is typically determined by reductions in quantitative spirometric indices, including forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (FVC) (Silverman et al., 2002; Celedon et al., 2004).

Most common symptoms of PULMONARY DISEASE, CHRONIC OBSTRUCTIVE; COPD

  • Asthma
  • Abnormal lung morphology
  • Emphysema
  • Bronchitis
  • Chronic lung disease


More info about PULMONARY DISEASE, CHRONIC OBSTRUCTIVE; COPD

SOURCES: OMIM

HEME OXYGENASE 1 DEFICIENCY; HMOX1D


Most common symptoms of HEME OXYGENASE 1 DEFICIENCY; HMOX1D

  • Growth delay
  • Anemia
  • Hepatomegaly
  • Fever
  • Proteinuria


More info about HEME OXYGENASE 1 DEFICIENCY; HMOX1D

SOURCES: OMIM MESH


Potential gene panels for HMOX1 gene

Pan-Ethnic Carrier Screen: Gene Sequencing Panel Panel

United States.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Pan-Ethnic Carrier Screen: Gene Sequencing Panel that also includes the following genes: RMRP BCS1L RS1 SACS BLM SGCA SGCB SGCG SGSH SLC12A6

More info about this panel

Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies Panel

United States.

By Mayo Clinic Genetic Testing Laboratories Mayo Clinic Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies that also includes the following genes: RHAG RPS19 SEC23B SLC2A1 SPTA1 SPTB TPI1 UGT1A1 XK CD59

More info about this panel

HMOX1 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the HMOX1 gene.

More info about this panel

Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis Panel

Canada.

By CEN4GEN Institute for Genomics and Molecular Diagnostics Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis that also includes the following genes: RMRP BCS1L SACS BLM SGCA SGCB SGCG SGSH SLC12A6 SLC17A5

More info about this panel


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