Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
R-numbers: R15 Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy, 612300, CD59 antigen P18-20 deficiency (CD59), Membrane Attack Complex Inhibitor (CD59) deficiency, Primary CD59 deficiency, paroxysmal nocturnal haemoglobinuria, chronic hemolysis, childhood relapsing immune-mediated polyneuropathy, Hemolytic anemia, polyneuropathy, Complement Deficiencies |
Green in Rare anaemiaR-numbers: R92 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 305000 Dyskeratosis congenita, X-linked, Dyskeratosis congenita, X-linked, 305000 |