Search Ontology:
Human Disease

immunodeficiency 112

Term ID
DOID:0061079
Synonyms
Definition
A T cell, B cell, and NK cell deficiency that is characterized by variable manifestations beginning in early childhood and that has_material_basis_in homozygous mutation in the MAP3K14 gene on chromosome 17q21. https://pubmed.ncbi.nlm.nih.gov/29230214/
References
Ontology
Human Disease   ( DOID:0061079 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models