Search Ontology:
Human Disease
agammaglobulinemia 8A
- Term ID
- DOID:0081140
- Synonyms
-
- Definition
- An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/32384040/
- References
- Ontology
- Human Disease ( DOID:0081140 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models