Search Ontology:
Human Disease

immunodeficiency 118

Term ID
DOID:0061084
Synonyms
Definition
A primary immunodeficiency disease that is characterized by increased susceptibility to the development of disseminated mycobacterial infections in infancy, notably after BCG vaccination and that has_material_basis_in hemizygous mutation in the MCTS1 gene on chromosome Xq24. https://pubmed.ncbi.nlm.nih.gov/37875108/
References
Ontology
Human Disease   ( DOID:0061084 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models