Meningioma
|
disease |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
634
|
43
|
0.100 |
None |
|
0 |
|
|
|
Neuroma
|
disease |
Neoplasms
|
Neoplastic Process
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Scoliosis, unspecified
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
850
|
135
|
0.100 |
None |
|
0 |
|
|
|
Focal T2 hyperintense brainstem lesion
|
phenotype |
|
Finding
|
33
|
2
|
0.100 |
None |
|
0 |
|
|
|
Intracranial Hypertension
|
disease |
Nervous System Diseases
|
Finding
|
72
|
1
|
0.100 |
None |
|
0 |
|
|
|
Arteriovenous Malformations, Cerebral
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
Congenital Abnormality
|
35
|
6
|
0.100 |
None |
|
0 |
1
|
|
|
Skin Diseases, Vascular
|
group |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
11
|
2
|
0.100 |
None |
|
0 |
|
|
|
Cavernous hemangioma of retina
|
disease |
Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Neoplastic Process
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Spinal cord lesion
|
phenotype |
Nervous System Diseases
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Venous malformation
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
38
|
3
|
0.100 |
None |
|
0 |
|
|
|
Somatic mutation
|
phenotype |
|
Cell or Molecular Dysfunction
|
151
|
|
0.100 |
None |
|
0 |
|
|
|
Impaired cognition
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
1630
|
348
|
0.100 |
None |
|
0 |
|
|
|
Hemangioma of choroid
|
disease |
Neoplasms; Cardiovascular Diseases
|
Neoplastic Process
|
4
|
2
|
0.100 |
None |
|
0 |
|
|
|
Paralysed
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
68
|
|
0.100 |
None |
|
0 |
|
|
|
Episodic vomiting
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
43
|
10
|
0.100 |
None |
|
0 |
|
|
|
Other malformations of cerebral vessels
|
disease |
|
Congenital Abnormality
|
2
|
|
0.200 |
None |
|
0 |
|
|
|
Focal T2 hypointense brainstem lesion
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the cerebrum
|
disease |
|
Anatomical Abnormality
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Cerebral Hemorrhage
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Pathologic Function
|
122
|
78
|
0.100 |
None |
|
0 |
|
|
|
Congenital abnormality of vein
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
39
|
7
|
0.100 |
None |
|
0 |
|
|
|
Nonruptured congenital cerebral aneurysm
|
disease |
|
Disease or Syndrome; Congenital Abnormality
|
2
|
|
0.200 |
None |
|
0 |
|
|
|
Congenital malformation of cerebral vessels NOS
|
disease |
|
Congenital Abnormality
|
2
|
|
0.200 |
None |
|
0 |
|
|
|
Cerebral Venous Angioma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases; Cardiovascular Diseases
|
Congenital Abnormality
|
4
|
|
0.200 |
None |
|
0 |
|
|
|
Headache
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
338
|
75
|
0.100 |
None |
|
0 |
|
|
|
Hemiparesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
91
|
6
|
0.100 |
None |
|
0 |
1
|
|
|