| Panel | Mode of inheritance | Details |
|---|---|---|
2 panels | ||
Green in Bleeding and platelet disordersR-numbers: R90 Signed-off version 4.16 | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Phenotypes 612416 Factor XI deficiency |
Green in Factor XI deficiencyR-numbers: R120 Signed-off version 1.4 | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Phenotypes Factor XI deficiency, autosomal dominant, OMIM:612416, Factor XI deficiency, autosomal recessive, OMIM:612416, congenital factor XI deficiency, MONDO:0012897 |