| Panel | Mode of inheritance | Details |
|---|---|---|
2 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 5.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Elliptocytosis-3, OMIM:617948, Anemia, neonatal hemolytic, fatal or near-fatal, OMIM:617948, Spherocytosis, type 2, OMIM:616649 |
Green in Rare anaemiaR-numbers: R92 Signed-off version 3.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Spherocytosis,616649, Elliptocytosis, Anemia, neonatal hemolytic, fatal and near-fatal, RBC membrane abnormality, 617948 Elliptocytosis-3, 616649 Spherocytosis, type 2, 616649 Anemia, neonatal hemolytic, fatal and near-fatal |