Ataxias, Hereditary
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
35
|
3
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Conn Adenoma
|
disease |
Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
107
|
5
|
0.010 |
None |
< 0.001 |
1 |
|
1995 |
1995 |
Purpura, Thrombotic Thrombocytopenic
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
80
|
13
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Friedreich Ataxia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
88
|
11
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Olivopontocerebellar Atrophies
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
28
|
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Cerebellar degeneration
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
60
|
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
|
disease |
Neoplasms
|
Neoplastic Process
|
95
|
1
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Congenital chromosomal disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
757
|
47
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Encephalopathies
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
457
|
64
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Adenocarcinoma of large intestine
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
543
|
432
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Ataxia Telangiectasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
384
|
698
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
TNF receptor-associated periodic fever syndrome (TRAPS)
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
90
|
33
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Progressive supranuclear palsy
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
176
|
52
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Plaque, Amyloid
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
123
|
10
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Congenital arteriovenous malformation
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
163
|
23
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Lewy Body Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
255
|
41
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Viral hepatitis
|
group |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
79
|
5
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Wiskott-Aldrich Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
95
|
34
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Drug Resistant Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
184
|
35
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Corticobasal degeneration
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
35
|
14
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Dentatorubral-Pallidoluysian Atrophy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
95
|
|
0.020 |
None |
1.000 |
2 |
|
2000 |
2001 |
Reticulosarcoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
80
|
2
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Alopecia, Male Pattern
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
91
|
743
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Androgenetic Alopecia
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
112
|
107
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
74
|
68
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |