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Metadata
ID	DOID:0061082
Name	immunodeficiency 116
Definition	A T cell deficiency that is characterized by the onset of recurrent upper and lower respiratory tract infections in infancy or early childhood and that has_material_basis_in homozygous mutation in the CD8-alpha gene on chromosome 2p12. https://pubmed.ncbi.nlm.nih.gov/26563160/
Xrefs	MIM:608957
Parent Relationships	is_a T cell deficiency 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