Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 2.1 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Fetal hydrops, Thalassemia, alpha-, 604131 |
Green in Hereditary ErythrocytosisR-numbers: R405 Signed-off version 1.19 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Erythrocytosis |
Green in Rare anaemiaR-numbers: R92 Signed-off version 2.1 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Hypochromic microcytic anemia, Heinz body anemia,140700, Globin Disorder, Erythrocytosis, Thalassemia, alpha-, 604131, 604131 Alpha thalassaemia, 60413 Thalassemia, alpha, Hemoglobin H disease, nondeletional, 613978 |