CDC73

cell division cycle 73
OMIM: 607393, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green CDC73 in Hypercalcaemia


Level 2: Endocrine disorders
Version 1.2

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperparathyroidism-jaw tumour syndrome, MIM# 145001
  • Hyperparathyroidism, familial primary, MIM# 145000

Green CDC73 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperparathyroidism-jaw tumour syndrome, MIM# 145001
  • Hyperparathyroidism, familial primary, MIM# 145000

Red CDC73 in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 0.131

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Parathyroid carcinoma, MIM# 608266

Green CDC73 in Calcium and Phosphate disorders


Level 2: Renal and urinary tract disorders; Endocrine disorders
Version 1.24

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • KidGen_CalcPhos v38.1.0
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperparathyroidism-jaw tumour syndrome, MIM# 145001
  • Hyperparathyroidism, familial primary, MIM# 145000

Green CDC73 in Renal Tubulopathies and related disorders


Level 2: Renal and urinary tract disorders
Version 1.18

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • KidGen_CalcPhos v38.1.0
    • Expert Review Green
    • Expert Review Green
    • Expert Review Green
    • KidGen_CalcPhos v38.1.0
    • Victorian Clinical Genetics Services
    Phenotypes
    • Hyperparathyroidism-jaw tumour syndrome, MIM# 145001
    • Hyperparathyroidism, familial primary, MIM# 145000

    Green CDC73 in Parathyroid Tumour


    Level 2: Cancer Predisposition
    Version 1.2

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Tumor of parathyroid gland, MONDO:0021360
    • Hyperparathyroidism 2 with jaw tumors, MONDO:0007768
    • Hyperparathyroidism-jaw tumor syndrome, MIM#145001
    • Hyperparathyroidism, familial primary, MIM#145000

    Red CDC73 in Wilms Tumour


    Level 2: Cancer Predisposition
    Version 1.0

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    • Expert Review
    • Expert list
    Phenotypes
    • Wilms tumor, MONDO:0006058
    • Hyperparathyroidism 2 with jaw tumors, MONDO:0007768
    • Hyperparathyroidism-jaw tumor syndrome, MIM#145001
    • Hyperparathyroidism, familial primary, MIM#145000