NDUFB7 gene related symptoms and diseases

All the information presented here about the NDUFB7 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.

Top 5 symptoms and clinical features associated to NDUFB7 gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Leukoencephalopathy Very Common - Between 80% and 100% cases
Pathologic fracture Very Common - Between 80% and 100% cases
Global brain atrophy Very Common - Between 80% and 100% cases
Oral-pharyngeal dysphagia Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with NDUFB7 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Personality changes
  • Abnormality of mitochondrial metabolism
  • Hypercalciuria
  • Back pain
  • Abnormality of the hand
  • Schizophrenia
  • Drooling
  • Leukopenia

And 94 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to NDUFB7 gene

Here you will find a list of rare diseases related to the NDUFB7. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


WILSON DISEASE


Alternate names

WILSON DISEASE Is also known as wd, hepatolenticular degeneration, wnd

Description

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Most common symptoms of WILSON DISEASE

  • Intellectual disability
  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Spasticity


More info about WILSON DISEASE

SOURCES: MESH OMIM ORPHANET


Potential gene panels for NDUFB7 gene

NDUFB7 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the NDUFB7 gene.

More info about this panel


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