Mental Retardation, X-Linked
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
141
13
0.020
None
1.000
2
1984
2000
Fragile X Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
194
11
0.020
None
1.000
2
1988
2001
Brain Diseases
group
Nervous System Diseases
Disease or Syndrome
345
10
0.010
None
1.000
1
2018
2018
Mental Retardation
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
505
98
0.010
None
1.000
1
2000
2000
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.300
strong
1.000
1
2019
2019
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
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
FRAXE Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
11
2
0.010
None
1.000
1
2001
2001
Multiple Chronic Conditions
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
929
42
0.010
None
1.000
1
2018
2018
Arthrogryposis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
198
33
0.110
None
1.000
1
2018
2018
Cardiovascular Diseases
group
Cardiovascular Diseases
Disease or Syndrome
1756
711
0.010
None
1.000
1
2017
2017
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
2000
2000
Malignant neoplasm of breast
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6941
3417
0.010
None
1.000
1
2017
2017
Lissencephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
71
9
0.100
None
0
Hand clenching
phenotype
Finding
26
9
0.100
None
0
Congenital Camptodactyly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
123
10
0.100
None
0
Byzanthine arch palate
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
Congenital Abnormality
497
70
0.100
None
0
Global developmental delay
disease
Mental or Behavioral Dysfunction
1825
553
0.100
None
0
Hypoplasia of scrotum
phenotype
Congenital Abnormality
57
3
0.100
None
0
Plagiocephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
74
12
0.100
None
0
Orbital separation diminished
phenotype
Finding
89
11
0.100
None
0
Upward slant of palpebral fissure
phenotype
Finding
216
16
0.100
None
0
Neuronal heterotopia
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
67
3
0.100
None
0
Clinodactyly of fingers
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
160
7
0.100
None
0
Cerebellar Hypoplasia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
Congenital Abnormality
226
26
0.100
None
0