Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in Rare anaemiaR-numbers: R92 Signed-off version 3.0 | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Phenotypes 182900 Spherocytosis, type 1, 182900 RBC membrane abnormality, RBC membrane abnormality, Spherocytosis, type 1,182900, Spherocytosis, type 1 |