| Metadata | |
|---|---|
| ID | DOID:0081140 |
| Name | agammaglobulinemia 8A |
| 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/ |
| Xrefs | |
| Parent Relationships |
is_a autosomal dominant disease is_a agammaglobulinemia |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |