Neoplasms
group
Neoplasms
Neoplastic Process
10161
1644
0.030
None
1.000
3
1997
2019
Intellectual Disability
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
2165
159
0.320
moderate
1.000
3
2017
2019
Malignant Neoplasms
group
Neoplasms
Neoplastic Process
8621
1641
0.020
None
1.000
2
2007
2019
Primary malignant neoplasm
group
Neoplasms
Neoplastic Process
8221
1374
0.020
None
1.000
2
2007
2019
Hypertensive disease
group
Cardiovascular Diseases
Disease or Syndrome
2322
1085
0.010
None
1.000
1
1
2019
2019
Skin Abnormalities
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Congenital Abnormality
106
16
0.300
moderate
1.000
1
2017
2017
Tongue Neoplasms
group
Neoplasms; Stomatognathic Diseases
Neoplastic Process
62
0.010
None
1.000
1
2009
2009
Neurologic Symptoms
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
233
30
0.010
None
1.000
1
2019
2019
Sarcoma
group
Neoplasms
Neoplastic Process
853
42
0.010
None
1.000
1
2017
2017
Malignant neoplasm of soft tissue
group
Neoplasms
Neoplastic Process
699
32
0.010
None
1.000
1
2017
2017
Muscle hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
967
579
0.300
moderate
1.000
1
2017
2017
Numbness
phenotype
Nervous System Diseases; Mental Disorders
Sign or Symptom
12
2
0.010
None
1.000
1
2017
2017
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2017
2017
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.300
moderate
1.000
1
2017
2017
Carcinogenesis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6243
355
0.010
None
1.000
1
2013
2013
Abnormality of the genital system
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
36
4
0.300
moderate
1.000
1
2017
2017
Sparse eyelashes
phenotype
Finding
60
4
0.100
None
0
Sparse body hair
phenotype
Finding
57
0.100
None
0
Hypotrichosis of the scalp
phenotype
Finding
12
1
0.100
None
0
Unspecified visual loss
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases
Sign or Symptom
235
11
0.100
None
0
Visual Impairment
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Finding
422
0.100
None
0
Abnormal vision
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Finding
115
6
0.100
None
0
Sparse and thin eyebrow
phenotype
Finding
68
8
0.100
None
0
Congenital cataract
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases
Congenital Abnormality
105
104
0.040
None
1.000
4
2
2015
2019
Alopecia
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
491
375
0.420
moderate
1.000
3
2017
2019