Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 3.3 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Angioedema, hereditary, types I and II 106100, Hereditary Angioedema (C1inh), Complement component 4, partial deficiency of 120790, Hereditary angioedema, Complement Deficiencies |