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
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
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
Maturation defect
phenotype
Acquired Abnormality
43
2
0.010
None
1.000
1
2017
2017
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
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
stage, colon cancer
phenotype
Digestive System Diseases; Neoplasms
Neoplastic Process
18
2
0.010
None
1.000
1
2010
2010
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
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
HOYERAAL-HREIDARSSON SYNDROME
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Hemic and Lymphatic Diseases; Behavior and Behavior Mechanisms
Disease or Syndrome
16
1
0.510
strong
1.000
1
2014
2014
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