Abnormal coordination
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
59
|
4
|
0.100 |
None |
|
0 |
|
|
|
Social and occupational deterioration
|
phenotype |
Mental Disorders
|
Finding
|
13
|
|
0.100 |
None |
|
0 |
|
|
|
Delusions
|
disease |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
62
|
15
|
0.100 |
None |
|
0 |
|
|
|
Negativism
|
phenotype |
Behavior and Behavior Mechanisms
|
Individual Behavior
|
12
|
|
0.100 |
None |
|
0 |
|
|
|
Gait Disturbance, CTCAE
|
phenotype |
|
Finding
|
299
|
|
0.100 |
None |
|
0 |
|
|
|
Microcephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
1064
|
27
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of metabolism/homeostasis
|
phenotype |
|
Finding
|
171
|
5
|
0.100 |
None |
|
0 |
|
|
|
Hyperhomocystinemia
|
phenotype |
|
Finding
|
11
|
1
|
0.100 |
None |
|
0 |
|
|
|
Childhood onset
|
phenotype |
|
Finding
|
56
|
|
0.100 |
None |
|
0 |
|
|
|
Muscle Weakness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
|
Sign or Symptom
|
536
|
87
|
0.100 |
None |
|
0 |
|
|
|
THROMBOPHILIA DUE TO THROMBIN DEFECT
|
phenotype |
|
Finding
|
4
|
2
|
0.300 |
None |
|
0 |
|
|
|
Addison Disease
|
disease |
Immune System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
111
|
13
|
0.100 |
None |
|
0 |
|
|
|
Hallucinations
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
178
|
18
|
0.100 |
None |
|
0 |
1
|
|
|
Recurrent thrombophlebitis
|
phenotype |
Cardiovascular Diseases
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Thromboembolism
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
25
|
3
|
0.100 |
None |
|
0 |
|
|
|
Gait abnormality
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
312
|
23
|
0.100 |
None |
|
0 |
|
|
|
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
|
disease |
|
Finding
|
11
|
30
|
0.100 |
None |
|
0 |
1
|
|
|
Coronary Stenosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
111
|
20
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Hyperthyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
279
|
27
|
0.200 |
None |
1.000 |
1 |
|
1994 |
1994 |
Hypothyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
613
|
283
|
0.200 |
None |
1.000 |
1 |
|
1994 |
1994 |
Arakawa syndrome 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2
|
1
|
0.020 |
None |
1.000 |
2 |
1
|
1997 |
1997 |
Methylcobalamin Deficiency, CblG Type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2
|
9
|
0.020 |
None |
1.000 |
2 |
1
|
1997 |
1997 |
Uremia
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
110
|
2
|
0.010 |
None |
< 0.001 |
1 |
|
1997 |
1997 |
Methylmalonic aciduria
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
33
|
4
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Methylmalonic acidemia
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
44
|
35
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |