Angle Closure Glaucoma
|
disease |
Eye Diseases
|
Disease or Syndrome
|
94
|
56
|
0.030 |
None |
1.000 |
3 |
|
2002 |
2019 |
Congenital chromosomal disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
757
|
47
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2017 |
Psoriasis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1308
|
705
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2017 |
Avellino corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
115
|
14
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2010 |
Anemia of chronic disease
|
phenotype |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
100
|
1
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2010 |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.700 |
None |
1.000 |
2 |
2
|
2014 |
2014 |
Amyloidosis cutis dyschromia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
84
|
1
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2010 |
stage, colon cancer
|
phenotype |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
18
|
2
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Maturation defect
|
phenotype |
|
Acquired Abnormality
|
43
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Neoplastic Process
|
2346
|
222
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Severe myopia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
184
|
116
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Congenital hypoplasia of adrenal gland
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
|
Congenital Abnormality
|
45
|
13
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Pancytopenia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
253
|
15
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
CUI: |
C0030193 |
Disease: |
Pain
|
Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
1554
|
196
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
X-linked Adrenal Hypoplasia
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
57
|
70
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.110 |
None |
1.000 |
1 |
|
2018 |
2018 |
Vitelliform Macular Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
74
|
120
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Lactic acidemia
|
phenotype |
|
Disease or Syndrome
|
12
|
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Dystrophy, granular
|
disease |
|
Disease or Syndrome
|
4
|
8
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Refractory Acute Lymphoblastic Leukemia
|
disease |
|
Neoplastic Process
|
14
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Familial Glucocorticoid Deficiency Type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
12
|
18
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Childhood Pre-B Acute Lymphoblastic Leukemia
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
51
|
3
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Childhood Leukemia
|
disease |
Neoplasms
|
Neoplastic Process
|
1740
|
140
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Familial Atypical Mole Melanoma Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
Neoplastic Process
|
30
|
3
|
0.300 |
None |
1.000 |
1 |
|
2015 |
2015 |
Hereditary Melanoma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
50
|
67
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |