Nephroblastoma
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Neoplastic Process
586
125
0.340
None
1.000
5
2008
2017
Bilateral Wilms Tumor
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
31
0.300
None
1.000
1
2017
2017
Kidney Diseases
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
1180
140
0.300
None
1.000
1
2008
2008
×
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
0.300
limited
1.000
1
2014
2014
Amyotrophic Lateral Sclerosis, Familial
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
130
68
0.300
None
1.000
1
2002
2002
Amyotrophic Lateral Sclerosis, Sporadic
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
173
90
0.300
None
1.000
1
2002
2002
AMYOTROPHIC LATERAL SCLEROSIS 1
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
164
139
0.300
None
1.000
1
2002
2002
Ptosis
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
607
12
0.110
None
1.000
1
2016
2016
Blepharoptosis
disease
Eye Diseases
Disease or Syndrome
595
57
0.110
None
1.000
1
2016
2016
Wide anterior fontanel
phenotype
Finding
71
5
0.100
None
0
Short Stature, CTCAE
phenotype
Finding
1010
0.100
None
0
Epicanthus inversus
phenotype
Finding
9
1
0.100
None
0
Frontal bossing
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
321
22
0.100
None
0
Macrocephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Congenital Abnormality
367
10
0.100
None
0
Small for gestational age (disorder)
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
Finding
181
34
0.100
None
0
High forehead
phenotype
Finding
211
17
0.100
None
0
Small for gestational age fetus
phenotype
Pathological Conditions, Signs and Symptoms
Finding
156
0.100
None
0
Absent/hypoplastic paranasal sinuses
phenotype
Finding
6
0.100
None
0
Short stature
phenotype
Finding
1127
292
0.100
None
0
Posteriorly rotated ear
disease
Congenital Abnormality
176
23
0.100
None
0
Depressed nasal bridge
phenotype
Finding
426
39
0.100
None
0
Premature posterior fontanelle closure
phenotype
Finding
1
0.100
None
0
Broad nasal tip
phenotype
Finding
125
8
0.100
None
0
Dwarfism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
Congenital Abnormality
1261
77
0.100
None
0
Abnormality of the skull base
disease
Anatomical Abnormality
2
0.100
None
0