NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
disease
Disease or Syndrome
1
16
0.700
strong
1.000
11
16
2011
2017
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
disease
Disease or Syndrome
1
2
0.600
strong
1.000
3
2
2013
2017
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE
disease
Disease or Syndrome
1
2
0.100
None
0
2
Bilateral polymicrogyria
disease
Congenital Abnormality
3
0.010
None
1.000
1
2018
2018
Delusion of persecution
disease
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
4
2
0.010
None
1.000
1
2006
2006
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Disease or Syndrome
4
18
0.010
None
1.000
1
2018
2018
Visual Cortex Disorder
disease
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Disease or Syndrome
7
0.010
None
1.000
1
2016
2016
Oculogyric crisis
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Pathologic Function
9
3
0.100
None
0
Trigeminal Neuralgia, Idiopathic
disease
Nervous System Diseases; Stomatognathic Diseases
Disease or Syndrome
12
0.300
None
1.000
1
2016
2016
Secondary Trigeminal Neuralgia
disease
Nervous System Diseases; Stomatognathic Diseases
Disease or Syndrome
12
0.300
None
1.000
1
2016
2016
Psychosis, Brief Reactive
disease
Mental Disorders
Mental or Behavioral Dysfunction
14
0.300
None
1.000
1
2004
2004
mass lesion
phenotype
Neoplastic Process
15
2
0.010
None
1.000
1
1997
1997
Nerve Pain
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
18
0.010
None
1.000
1
2017
2017
Schizophreniform Disorders
group
Mental Disorders
Mental or Behavioral Dysfunction
20
1
0.300
None
1.000
1
2004
2004
Dystonia Musculorum Deformans
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
26
1
0.010
None
1.000
1
1993
1993
Shared Paranoid Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
27
10
0.010
None
< 0.001
1
2018
2018
Expressive language delay
phenotype
Disease or Syndrome
30
25
0.100
None
0
1
Involuntary Movements
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
37
5
0.410
strong
1.000
2
2015
2017
Anti-N-Methyl-D-Aspartate Receptor Encephalitis
disease
Neoplasms; Immune System Diseases; Nervous System Diseases
Disease or Syndrome
43
0.090
None
0.889
9
2012
2019
Placental Insufficiency
disease
Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
45
0.200
None
1.000
1
2009
2009
Epilepsy, Rolandic
disease
Nervous System Diseases
Disease or Syndrome
46
81
0.100
None
1.000
1
1
2018
2018
Hashimoto's encephalitis
disease
Nervous System Diseases; Endocrine System Diseases
Disease or Syndrome
47
0.010
None
1.000
1
2019
2019
×
CUI:
C0234238
Disease:
Ache
Ache
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
50
0.300
None
1.000
1
2008
2008
Pain, Splitting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
50
0.300
None
1.000
1
2008
2008
Pain, Crushing
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
50
0.300
None
1.000
1
2008
2008