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1 OMIM reference -
1 associated gene
5 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Pyogenic bacterial infections due to MyD88 deficiency
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency

MYD88 IRAK4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MYD88
(0.89)
IRAK4



Citations in the biomedical literature:


Pyogenic bacterial infections due to MyD88 deficiency
MYD88
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency
IRAK4



Pyogenic bacterial infections due to MyD88 deficiency
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency

Synonym(s):
- MyD88 deficiency

Synonym(s):
- IRAK4 deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: any age
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Immunodeficiency / increased susceptibility to infections / recurrent infections


Pyogenic bacterial infections due to MyD88 deficiency
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency

Very frequent
- Autosomal recessive inheritance

Frequent
- Chronic skin infection / ulcerations / ulcers / cancrum
- Nasal congestion / sinusitis / rhinitis / rhinorrhea

Occasional
- Fever / chilling


Very frequent
- Anomalies of the lymphatic system
- Polynuclear cells / neutrophils anomalies / neutropenia