Search Ontology:
Human Disease

immunodeficiency 116

Term ID
DOID:0061082
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0061082 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models