Term Name: immunodeficiency 106
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.
Ontology: Human Disease [DOID:0061075]   ( DOID:0061075 )

Relationships
is a type of: autosomal recessive disease primary immunodeficiency disease