Autosomal dominant tubulointerstitial kidney disease
disease
Disease or Syndrome
13
3
0.040
None
1.000
4
2003
2019
Autosomal Recessive Polycystic Kidney Disease
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
69
317
0.030
None
1.000
3
2004
2016
Benign Prostatic Hyperplasia
disease
Male Urogenital Diseases
Disease or Syndrome
770
91
0.100
None
1.000
1
1
2018
2018
Bicornuate uterus
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Congenital Abnormality
44
0.100
None
0
bilateral agenesis
disease
Congenital Abnormality
2
0.010
None
1.000
1
2013
2013
Bilateral Multicystic Dysplastic Kidneys
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome; Congenital Abnormality
1
0.300
None
1.000
2
2010
2013
Biliary Atresia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Congenital Abnormality
184
32
0.010
None
1.000
1
2019
2019
Biliary calculi
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Body Substance
48
31
0.100
None
1.000
1
1
2018
2018
Biliary tract abnormality
phenotype
Digestive System Diseases
Finding
14
0.100
None
0
Biliary Tract Cancer
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
167
11
0.010
None
1.000
1
2012
2012
Blepharophimosis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Congenital Abnormality
106
15
0.020
None
0.500
2
2004
2009
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder)
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases
Disease or Syndrome
9
92
0.010
None
1.000
1
2014
2014
Blood urea nitrogen measurement
phenotype
Laboratory Procedure
90
174
0.100
None
1.000
2
1
2018
2019
Body mass index
phenotype
Clinical Attribute
1014
2689
0.100
None
1.000
1
2
2017
2017
BPES type I
disease
Disease or Syndrome
2
1
0.010
None
1.000
1
2014
2014
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
0.100
None
1.000
1
1
2016
2016
×
CUI:
C1968949
Disease:
Cakut
Cakut
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
72
8
0.080
None
1.000
8
2010
2019
Carcinogenesis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6243
355
0.050
None
1.000
5
2005
2019
Carcinoma
group
Neoplasms
Neoplastic Process
2462
103
0.040
None
1.000
4
2005
2019
Carcinoma of lung
disease
Neoplasms; Respiratory Tract Diseases
Neoplastic Process
4081
1204
0.100
None
1.000
1
2
2016
2016
Carcinoma, Endometrioid
disease
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Neoplastic Process
223
12
0.020
None
1.000
2
2016
2019
Carcinoma, Ovarian Epithelial
disease
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Neoplastic Process
2841
327
0.080
None
1.000
8
3
2003
2020
Carcinoma, Transitional Cell
disease
Neoplasms
Neoplastic Process
623
12
0.010
None
1.000
1
2017
2017
Cardiovascular Abnormalities
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
99
12
0.010
None
1.000
1
2014
2014
Cerebral atrophy
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
454
44
0.100
None
0