Nephrotic Syndrome
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
384
45
0.140
None
1.000
4
1
2006
2017
Eye Abnormalities
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Congenital Abnormality
55
3
0.020
None
1.000
2
2006
2006
Congenital Abnormality
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
1098
73
0.010
None
1.000
1
2009
2009
Brain Neoplasms
group
Neoplasms; Nervous System Diseases
Neoplastic Process
1018
204
0.010
None
1.000
1
2006
2006
Cognition Disorders
group
Mental Disorders
Mental or Behavioral Dysfunction
607
47
0.300
None
1.000
1
2018
2018
Kidney Diseases
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
1180
140
0.010
None
1.000
1
2006
2006
Prostatic Neoplasms
group
Neoplasms; Male Urogenital Diseases
Neoplastic Process
1722
31
0.300
None
1.000
1
2007
2007
Retinal Diseases
group
Eye Diseases
Disease or Syndrome
714
56
0.010
None
1.000
1
2011
2011
Intellectual Disability
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
2165
159
0.110
None
1.000
1
2008
2008
Deglutition Disorders
group
Digestive System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
389
50
0.100
None
0
Myopathy
group
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
634
166
0.100
None
0
Proteinuria
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
239
20
0.300
None
1.000
1
2011
2011
Sclerosis
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
24
0.010
None
1.000
1
2004
2004
Familial mesangial sclerosis
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
1
0.300
None
1.000
1
2004
2004
Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases
Disease or Syndrome
1
0.300
None
1.000
1
2004
2004
Unspecified visual loss
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases
Sign or Symptom
235
11
0.010
None
1.000
1
2006
2006
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0
Muscle hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
967
579
0.100
None
0
Hyporeflexia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
312
0.100
None
0
Proximal muscle weakness
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Finding
112
11
0.100
None
0
Waddling gait
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
113
8
0.100
None
0
Dyspnea on exertion
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
102
3
0.100
None
0
Absent reflex
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
201
16
0.100
None
0
Weak cry
phenotype
Finding
42
4
0.100
None
0
Difficulty chewing
phenotype
Finding
14
0.100
None
0