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Metadata
ID	DOID:0061075
Name	immunodeficiency 106
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/
Xrefs	MIM:619935
Parent Relationships	is_a primary immunodeficiency disease is_a autosomal recessive disease
Subclass Logical Relationships	existence starts during some (Infantile onset or Childhood onset) has material basis in some autosomal recessive inheritance