immunodeficiency 106

Term ID

DOID:0061075

Synonyms

Definition

A primary immunodeficiency disease that is characterized by increased susceptibility to viral infections beginning in infancy or early childhood and that has_material_basis_in homozygous or compound heterozygous mutation in the IFNAR1 gene on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/35442418/

References

MIM:619935

Ontology

Human Disease ( DOID:0061075 )

Relationships

is a type of: autosomal recessive disease primary immunodeficiency disease

autosomal recessive disease primary immunodeficiency disease Show first 5 Terms

Other Pages

Genes Involved

Zebrafish Models