Charcot-Marie-Tooth disease, Type 2D
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
5
|
9
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Finnish congenital nephrotic syndrome
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
11
|
178
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Agyria
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
20
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
CRANIOSYNOSTOSIS, TYPE 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
23
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Neuropsychiatric Systemic Lupus Erythematosus
|
disease |
Infections; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
33
|
3
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Chills
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
34
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Cockayne Syndrome, Type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
34
|
69
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
34
|
6
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Giardiasis
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
48
|
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Paracoccidioidomycosis
|
disease |
Infections
|
Disease or Syndrome
|
50
|
5
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Dysautonomia, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome; Congenital Abnormality
|
52
|
46
|
0.020 |
None |
0.500 |
2 |
|
2011 |
2018 |
Polycystic Kidney - body part
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Anatomical Abnormality
|
54
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
stage, prostate cancer
|
disease |
Neoplasms; Male Urogenital Diseases
|
Neoplastic Process
|
58
|
5
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Malaria, Vivax
|
disease |
Infections
|
Disease or Syndrome
|
60
|
2
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Post-Traumatic Osteoporosis
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
61
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Lissencephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
71
|
9
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2010 |
Osteoporosis, Senile
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
73
|
3
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Atypical Ductal Breast Hyperplasia
|
disease |
Neoplasms
|
Neoplastic Process
|
80
|
17
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Iron deficiency anemia
|
disease |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
83
|
21
|
0.010 |
None |
< 0.001 |
1 |
|
2018 |
2018 |
Osteoporosis, Age-Related
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
89
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Traditional Serrated Adenoma
|
disease |
Neoplasms
|
Neoplastic Process
|
90
|
2
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Thrombocytosis
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
93
|
12
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Macular dystrophy, corneal type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
100
|
54
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Congenital anomaly of brain
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases
|
Congenital Abnormality
|
103
|
7
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Osteitis Deformans
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
134
|
58
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |