elevated blood glucose level
|
phenotype |
|
Finding
|
89
|
111
|
0.100 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
mathematical ability
|
phenotype |
|
Mental Process
|
854
|
2127
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Glucose measurement
|
phenotype |
|
Laboratory Procedure
|
89
|
111
|
0.100 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
Insulin measurement
|
phenotype |
|
Laboratory Procedure
|
15
|
25
|
0.100 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
Hallervorden-Spatz Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
22
|
42
|
0.060 |
None |
1.000 |
6 |
|
2001 |
2018 |
Neurodegeneration with brain iron accumulation (NBIA)
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
40
|
2
|
0.020 |
None |
1.000 |
2 |
|
2010 |
2012 |
Parkinsonian Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
373
|
95
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2010 |
Neurodegenerative Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
1515
|
85
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Primary malignant neoplasm
|
group |
Neoplasms
|
Neoplastic Process
|
8221
|
1374
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Spondyloepiphyseal dysplasia, Omani type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
3
|
16
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Neuroferritinopathy
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
17
|
5
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Spastic paraplegia 11, autosomal recessive
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
9
|
134
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Spastic paraplegia type 5A, recessive
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
13
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Ataxia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
868
|
68
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Dystonia Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
167
|
37
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Malignant Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
8621
|
1641
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Cerebellar Ataxia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
441
|
120
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Dystonia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
453
|
97
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Hallermann's Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
13
|
1
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Parkinson Disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
2078
|
990
|
0.010 |
None |
< 0.001 |
1 |
|
2005 |
2005 |
Staphylococcal Infections
|
group |
Infections
|
Disease or Syndrome
|
37
|
5
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Infantile Neuroaxonal Dystrophy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
17
|
25
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Hypoplasia of corpus callosum
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
385
|
49
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Malignant tumor of exocrine pancreas
|
disease |
Digestive System Diseases; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |