| Panel | Mode of inheritance | Details |
|---|---|---|
5 panels | ||
Signed-off version 2.2 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Hyperparathyroidism-Jaw Tumor Syndrome |
Green in Childhood solid tumoursSigned-off version 5.11 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes 145001 |
Green in Endocrine neoplasiaR-numbers: R217 Signed-off version 3.8 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Endocrine Cancer |
R-numbers: R151 Signed-off version 3.10 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Hyperparathyroidism, familial primary (145000), Hyperparathyroidism-jaw tumor syndrome (145001) |
Green in Inherited parathyroid cancerR-numbers: R226 Signed-off version 1.4 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Hyperparathyroidism-jaw tumor syndrome, OMIM:145001, Parathyroid adenoma with cystic changes, OMIM:145001, Parathyroid carcinoma, OMIM:608266, parathyroid gland carcinoma, MONDO:0012004 |