KL

klotho
OMIM: 604824, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber KL in Hypophosphataemia or rickets


Level 2: Endocrine disorders; Skeletal disorders
Version 1.0

1 review Unknown
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services

Amber KL in Mendeliome


Version 2.0

1 review Unknown
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Tumoral calcinosis, hyperphosphatemic, familial, 3 MIM#617994
  • Hyperphosphatemia

Amber KL in Renal Tubulopathies and related disorders


Level 2: Renal and urinary tract disorders
Version 2.0

1 review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • KidGen_CalcPhos v38.1.0
  • Expert Review Amber
Phenotypes
  • Hyperphosphatemia
  • Tumoral calcinosis, hyperphosphatemic, familial, 3 MIM#617994