Renal Tubulopathies and related disorders
Gene: MEN1
Hypercalcaemia is a prominent feature of familial hyperparathyroidism that has been caused by MEN1 in at least 5 cases.
Sources: Expert listCreated: 28 Nov 2022, 6 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Multiple endocrine neoplasia 1 MIM#131100
Publications
Comment on list classification: Gene requested by endocrinologists at RMH to be on this panelCreated: 6 Feb 2020, 11:14 a.m. | Last Modified: 6 Feb 2020, 11:14 a.m.
Panel Version: 0.7
Hypercalcaemia is a prominent feature of familial hyperparathyroidism that has been caused by MEN1 in at least 5 cases.
Sources: Expert listCreated: 6 Feb 2020, 11:11 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Multiple endocrine neoplasia 1 MIM#131100
Publications
gene: MEN1 was added gene: MEN1 was added to Renal Tubulopathies and related disorders. Sources: Expert list,Expert Review Green Mode of inheritance for gene: MEN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MEN1 were set to 31797261, 14985373 Phenotypes for gene: MEN1 were set to Multiple endocrine neoplasia 1 MIM#131100