Senile Plaques
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
249
|
21
|
0.110 |
None |
1.000 |
1 |
|
2017 |
2017 |
Middle Cerebral Artery Occlusion
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Acquired Abnormality
|
626
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Glial scar
|
phenotype |
|
Acquired Abnormality
|
51
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Surgically-Created Resection Cavity
|
disease |
|
Acquired Abnormality
|
16
|
3
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Plaque, Amyloid
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
123
|
10
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Coloboma of iris
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Anatomical Abnormality
|
153
|
12
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Vegetation
|
disease |
|
Anatomical Abnormality
|
67
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Abnormal brain FDG positron emission tomography
|
disease |
|
Anatomical Abnormality
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Nerve Degeneration
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
165
|
17
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Neurofibrillary degeneration (morphologic abnormality)
|
phenotype |
|
Cell or Molecular Dysfunction
|
21
|
|
0.100 |
None |
|
0 |
|
|
|
Congenital contractural arachnodactyly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
559
|
48
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Frontotemporal dementia
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
320
|
215
|
0.900 |
strong |
0.976 |
211 |
27
|
2006 |
2020 |
GRN-related frontotemporal dementia
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
112
|
20
|
0.100 |
None |
0.990 |
100 |
3
|
2006 |
2020 |
Pick Disease of the Brain
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
213
|
83
|
0.100 |
None |
0.977 |
86 |
3
|
2006 |
2020 |
Alzheimer's Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
3397
|
1843
|
0.200 |
None |
0.970 |
66 |
8
|
2006 |
2019 |
Neurodegenerative Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
1515
|
85
|
0.100 |
None |
0.952 |
63 |
3
|
2006 |
2020 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.100 |
None |
1.000 |
28 |
|
2007 |
2019 |
Neuronal Ceroid-Lipofuscinoses
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
51
|
74
|
0.100 |
None |
1.000 |
25 |
1
|
2012 |
2019 |
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
|
disease |
|
Disease or Syndrome
|
8
|
23
|
0.980 |
moderate |
1.000 |
24 |
23
|
2006 |
2018 |
Amyotrophic Lateral Sclerosis
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1114
|
485
|
0.100 |
None |
0.955 |
22 |
5
|
2007 |
2018 |
Obesity
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2821
|
1111
|
0.100 |
None |
0.929 |
14 |
|
2003 |
2019 |
Lysosomal Storage Diseases
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
130
|
8
|
0.100 |
None |
0.929 |
14 |
|
2014 |
2019 |
CEROID LIPOFUSCINOSIS, NEURONAL, 11
|
disease |
|
Disease or Syndrome
|
1
|
8
|
0.700 |
None |
1.000 |
13 |
8
|
2006 |
2017 |
Parkinson Disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
2078
|
990
|
0.100 |
None |
0.917 |
12 |
3
|
2007 |
2018 |
Parkinsonian Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
373
|
95
|
0.200 |
None |
1.000 |
11 |
1
|
2006 |
2018 |