IL12A-AS1 gene related symptoms and diseases

All the information presented here about the IL12A-AS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to IL12A-AS1 gene

Symptoms // Phenotype % Cases
Seizures Very Common - Between 80% and 100% cases
Glomerulopathy Very Common - Between 80% and 100% cases
Raynaud phenomenon Very Common - Between 80% and 100% cases
Gangrene Very Common - Between 80% and 100% cases
Pulmonary infiltrates Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with IL12A-AS1 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Pustule
  • Uveitis
  • Aseptic necrosis
  • Pulmonary embolism
  • Hemoptysis
  • Pericarditis
  • Keratoconjunctivitis sicca
  • Blurred vision

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

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Rare diseases associated to IL12A-AS1 gene

Here you will find a list of rare diseases related to the IL12A-AS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


BEHÇET DISEASE


Alternate names

BEHÇET DISEASE Is also known as bd, behcet disease

Description

Behçet's disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.

Most common symptoms of BEHÇET DISEASE

  • Seizures
  • Ataxia
  • Neoplasm
  • Pain
  • Cataract


More info about BEHÇET DISEASE

SOURCES: OMIM ORPHANET MESH




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