CST3, cystatin C, 1471

N. diseases: 370; N. variants: 10
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: C4055183
Disease: Contrast - Induced Nephropathy
Contrast - Induced Nephropathy
disease Disease or Syndrome 19 0.070 None 1.000 7 2017 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.050 None 0.800 5 1999 2018
CUI: C1619716
Disease: Cystatin C measurement
Cystatin C measurement
phenotype Laboratory Procedure 2 8 0.100 None 1.000 3 3 2010 2017
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.030 None 1.000 3 2017 2019
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy
disease Disease or Syndrome 138 21 0.030 None 1.000 3 2016 2018
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.020 None 1.000 2 1989 2006
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1
disease Disease or Syndrome 10 1 0.020 None 1.000 2 2002 2009
ST-segment elevation myocardial infarction (STEMI)
disease Disease or Syndrome 51 2 0.020 None 1.000 2 2017 2019
CUI: C0282667
Disease: Infant, Very Low Birth Weight
Infant, Very Low Birth Weight
disease Disease or Syndrome 26 1 0.010 None 1.000 1 2017 2017
CUI: C0442833
Disease: Arteriolar hyalinosis
Arteriolar hyalinosis
disease Acquired Abnormality 7 0.010 None 1.000 1 2018 2018
CUI: C0578575
Disease: Dissection of proximal aorta
Dissection of proximal aorta
disease Disease or Syndrome 26 0.010 None 1.000 1 2017 2017
CUI: C0852283
Disease: Respiratory Distress Syndrome
Respiratory Distress Syndrome
disease Disease or Syndrome 58 9 0.010 None 1.000 1 2018 2018
Congenital urinary tract obstruction
disease Congenital Abnormality 2 0.010 None 1.000 1 2019 2019
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder
phenotype Disease or Syndrome 171 1 0.010 None < 0.001 1 1 2013 2013
[D]Sleep disturbances (& [hypersomnia] or [insomnia])
phenotype Sign or Symptom 69 23 0.010 None 1.000 1 2018 2018
CUI: C1301700
Disease: Cardiovascular morbidity
Cardiovascular morbidity
phenotype Disease or Syndrome 75 2 0.010 None 1.000 1 2017 2017
Differentiated Thyroid Gland Carcinoma
disease Neoplastic Process 245 80 0.010 None 1.000 1 2019 2019
CUI: C1402315
Disease: Vascular lesions
Vascular lesions
disease Disease or Syndrome 111 9 0.010 None 1.000 1 2017 2017
CUI: C1504438
Disease: Cerebral artery stenosis
Cerebral artery stenosis
disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1609524
Disease: ADHF
ADHF
disease Disease or Syndrome 46 0.010 None 1.000 1 2019 2019
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer
disease Neoplastic Process 398 7 0.010 None < 0.001 1 2017 2017
CUI: C2363915
Disease: Cerebellar ischaemia
Cerebellar ischaemia
disease Disease or Syndrome 4 0.010 None 1.000 1 2015 2015
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 1 2018 2018
Non ST segment elevation acute coronary syndrome
disease Disease or Syndrome 12 2 0.010 None 1.000 1 2019 2019
CUI: C3714753
Disease: RETINOSCHISIS 1, X-LINKED, JUVENILE
RETINOSCHISIS 1, X-LINKED, JUVENILE
disease Disease or Syndrome 33 59 0.010 None 1.000 1 2020 2020