FGF23, fibroblast growth factor 23, 8074

N. diseases: 305; N. variants: 19
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia 		disease Congenital Abnormality 53 5 0.090 None 1.000 9 2003 2018
CUI: C1301700
Disease: Cardiovascular morbidity
Cardiovascular morbidity 		phenotype Disease or Syndrome 75 2 0.060 None 1.000 6 2014 2019
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis 		disease Disease or Syndrome 297 3 0.040 None 1.000 4 2016 2019
CUI: C1442839
Disease: Hypervitaminosis D
Hypervitaminosis D 		disease Disease or Syndrome 2 0.040 None 1.000 4 2006 2014
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.040 None 1.000 4 2005 2012
CUI: C4693863
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		disease Disease or Syndrome 1 4 0.600 strong 1.000 4 4 2005 2014
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.030 None 1.000 3 2018 2019
CUI: C1831619
Disease: Phosphaturic Mesenchymal Tumor
Phosphaturic Mesenchymal Tumor 		disease Neoplastic Process 6 0.030 None 1.000 3 2017 2019
CUI: C4692564
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1 		disease Disease or Syndrome 3 18 0.600 strong 1.000 3 3 2005 2011
CUI: C1142276
Disease: Renal anemia
Renal anemia 		disease Disease or Syndrome 12 0.020 None 1.000 2 2017 2018
CUI: C3814879
Disease: Phosphaturic mesenchymal tumor, benign
Phosphaturic mesenchymal tumor, benign 		disease Neoplastic Process 3 0.020 None 1.000 2 2018 2019
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease Anatomical Abnormality 148 18 0.020 None 0.500 2 2002 2017
CUI: C4048329
Disease: Immunosuppression
Immunosuppression 		disease Disease or Syndrome 632 9 0.020 None 1.000 2 2017 2019
CUI: C4087411
Disease: Oncogenic hypophosphataemic osteomalacia
Oncogenic hypophosphataemic osteomalacia 		disease Disease or Syndrome 5 0.020 None 1.000 2 2001 2003
CUI: C0239337
Disease: Deformity of limb
Deformity of limb 		group Anatomical Abnormality 37 3 0.010 None 1.000 1 2004 2004
CUI: C0240225
Disease: Liver mass
Liver mass 		phenotype Disease or Syndrome 36 0.010 None 1.000 1 2018 2018
CUI: C0342951
Disease: Hypervitaminosis
Hypervitaminosis 		phenotype Disease or Syndrome 4 0.010 None 1.000 1 2009 2009
CUI: C0428796
Disease: Senile sclerosis of aortic cusp
Senile sclerosis of aortic cusp 		disease Disease or Syndrome 19 0.010 None 1.000 1 2014 2014
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease 		phenotype Neoplastic Process 384 40 0.010 None 1.000 1 2018 2018
CUI: C0743323
Disease: Acute dyspnea
Acute dyspnea 		phenotype Sign or Symptom 4 0.010 None 1.000 1 2018 2018
CUI: C0748168
Disease: Pulmonary Pathology
Pulmonary Pathology 		disease Disease or Syndrome 29 0.010 None 1.000 1 2019 2019
CUI: C1336052
Disease: Spindle Cell Neoplasm
Spindle Cell Neoplasm 		disease Neoplastic Process 19 0.010 None 1.000 1 2018 2018
CUI: C1579029
Disease: Chronic uremia
Chronic uremia 		disease Disease or Syndrome 5 0.010 None 1.000 1 2014 2014
CUI: C1963961
Disease: Testosterone deficiency
Testosterone deficiency 		disease Disease or Syndrome 24 1 0.010 None 1.000 1 2019 2019
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis 		phenotype Disease or Syndrome 328 0.010 None 1.000 1 2018 2018