Intellectual Disability
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
2165
159
0.070
None
0.857
7
2004
2019
Mental Retardation, X-Linked Nonsyndromic
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
16
2
0.300
moderate
1.000
7
1993
2015
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
0.030
None
1.000
3
2004
2008
Mental Retardation, X-Linked
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
141
13
0.030
None
1.000
3
2004
2008
Impaired cognition
disease
Mental Disorders
Mental or Behavioral Dysfunction
1630
348
0.020
None
1.000
2
2008
2019
Mental Retardation, X-Linked 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
45
29
0.310
None
1.000
2
2002
2008
Guillain-Barre Syndrome, Familial
disease
Immune System Diseases; Nervous System Diseases
Disease or Syndrome
54
0.010
None
1.000
1
2003
2003
Group B Streptococcal Infection
disease
Infections
Disease or Syndrome
55
0.010
None
1.000
1
2003
2003
Liver carcinoma
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
5725
942
0.010
None
1.000
1
2019
2019
Guillain-Barre Syndrome
disease
Immune System Diseases; Nervous System Diseases
Disease or Syndrome
163
13
0.010
None
1.000
1
2003
2003
Hyperglycemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
1098
108
0.010
None
1.000
1
2017
2017
Mental Retardation, X-Linked 9
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
5
0.500
strong
1.000
1
2004
2004
Trichohepatoenteric Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
Disease or Syndrome
424
28
0.010
None
1.000
1
2015
2015
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2019
2019
Obesity
disease
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
Disease or Syndrome
2821
1111
0.110
None
1.000
1
2017
2017
Epilepsy
disease
Nervous System Diseases
Disease or Syndrome
1215
339
0.010
None
1.000
1
2015
2015
Tumor Cell Invasion
phenotype
Neoplastic Process
6626
169
0.010
None
1.000
1
2003
2003
Midface retrusion
phenotype
Finding
228
0.100
None
0
Long palpebral fissure
phenotype
Finding
73
10
0.100
None
0
X- linked recessive
phenotype
Finding
172
1
0.100
None
0
Poor speech
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
208
9
0.100
None
0
Widened subarachnoid space
phenotype
Finding
35
1
0.100
None
0
Periorbital fullness
phenotype
Finding
57
4
0.100
None
0
2-3 toe syndactyly
disease
Congenital Abnormality
85
16
0.100
None
0
Moderate sensorineural hearing impairment
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Finding
34
1
0.100
None
0