Genomics England
GMS Panels
Panels
Genes and Entities

FGF23

fibroblast growth factor 23
OMIM: 605380
PanelMode of inheritanceDetails
4 panels
Green
in Familial tumoral calcinosis
R-numbers: R162
Signed-off version 1.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Tumoral calcinosis, hyperphosphatemic, familial, 2, 617993
Green
in Hypophosphataemia or rickets
R-numbers: R154
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Hypophosphatemic rickets, autosomal dominant (193100)
Green
in Pigmentary skin disorders
R-numbers: R236
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Familial tumoural calcinosis, ADHR, TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2, HFTC2, HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 4.31
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Hypophosphatemic rickets, autosomal dominant 193100, Osteomalacia, tumor-induced, Tumoral calcinosis, hyperphosphatemic, familial 211900