Search Ontology:
Human Disease

immunodeficiency 129

Term ID
DOID:0061094
Synonyms
Definition
A T cell deficiency that is characterized by recurrent bacterial, viral, and fungal infections beginning in the first or second decades of life and that has_material_basis_in homozygous mutation in the RHOH gene on chromosome 4p14. https://pubmed.ncbi.nlm.nih.gov/38775840/
References
Ontology
Human Disease   ( DOID:0061094 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models