×
CUI:
C0018099
Disease:
Gout
Gout
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
205
2354
0.100
None
1.000
2
10
2010
2013
Retinitis Pigmentosa
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Disease or Syndrome
546
541
0.410
None
1.000
2
2015
2019
RETINITIS PIGMENTOSA 71
disease
Disease or Syndrome
2
7
0.700
strong
1.000
2
7
2013
2015
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
2013
2013
Cholera
disease
Infections
Disease or Syndrome
209
1
0.010
None
1.000
1
2018
2018
VATER Association
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
Disease or Syndrome
12
0.200
None
1.000
1
2011
2011
Jeune thoracic dystrophy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Disease or Syndrome
29
116
0.500
strong
1.000
1
2013
2013
Somatotropin deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
Disease or Syndrome
154
14
0.010
None
1.000
1
2015
2015
Nijmegen Breakage Syndrome
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
94
144
0.010
None
1.000
1
2016
2016
Familial aplasia of the vermis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases
Disease or Syndrome
95
187
0.100
None
1.000
1
1
2015
2015
Blindness
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Disease or Syndrome
393
34
0.110
None
1.000
1
2018
2018
VACTERL Association With Hydrocephalus
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
5
7
0.010
None
1.000
1
2011
2011
Mainzer-Saldino Disease
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Disease or Syndrome
5
20
0.510
strong
1.000
1
2013
2013
Isolated somatotropin deficiency
disease
Disease or Syndrome
168
27
0.010
None
1.000
1
2015
2015
SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY
disease
Disease or Syndrome
2
8
0.600
strong
1.000
1
8
2013
2013
Cholestasis
disease
Digestive System Diseases
Disease or Syndrome
420
15
0.100
None
0
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.100
None
0
Glaucoma
disease
Eye Diseases
Disease or Syndrome
770
198
0.100
None
0
Conductive hearing loss
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
291
5
0.100
None
0
Sensorineural Hearing Loss (disorder)
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
783
111
0.100
None
0
Hyperinsulinism
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
620
64
0.100
None
0
Hypertensive disease
group
Cardiovascular Diseases
Disease or Syndrome
2322
1085
0.100
None
0
Hypogonadism
disease
Endocrine System Diseases
Disease or Syndrome
305
24
0.100
None
0
Keratoconus
disease
Eye Diseases
Disease or Syndrome
269
83
0.100
None
0
Kidney Diseases
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
1180
140
0.100
None
0