Glycogen Storage Disease Type VII
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
9
9
0.940
None
1.000
17
9
1990
2016
Glycogen Storage Disease
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
63
16
0.400
limited
1.000
3
1
1994
1997
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.020
None
1.000
2
1997
1999
Renal tubular acidosis
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
52
3
0.010
None
1.000
1
2008
2008
Hyperglycemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
1098
108
0.010
None
1.000
1
2019
2019
Myopathy
group
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
634
166
0.010
None
1.000
1
1995
1995
Tuberculosis
disease
Infections
Disease or Syndrome
1256
328
0.010
None
1.000
1
2013
2013
Urinary tract infection
group
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases
Disease or Syndrome
219
14
0.010
None
1.000
1
2019
2019
Myocardial Ischemia
disease
Cardiovascular Diseases
Disease or Syndrome
756
103
0.300
None
1.000
1
2005
2005
Neuromuscular inhibition
disease
Disease or Syndrome
72
2
0.010
None
1.000
1
2017
2017
Disorder of purine metabolism
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
7
0.010
None
1.000
1
2017
2017
Disorder of fatty acid metabolism
group
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
6
0.010
None
1.000
1
2017
2017
Impaired insulin secretion
disease
Disease or Syndrome
88
14
0.010
None
1.000
1
1997
1997
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
0.100
None
0
Anemia, Hemolytic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
154
31
0.100
None
0
Cholelithiasis
disease
Digestive System Diseases
Disease or Syndrome
252
90
0.100
None
0
×
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
0
Hyperuricemia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
196
76
0.100
None
0
Alloxan Diabetes
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Experimental Model of Disease
112
0.300
None
1.000
1
2004
2004
Diabetes Mellitus, Experimental
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Experimental Model of Disease
522
0.300
None
1.000
1
2004
2004
Streptozotocin Diabetes
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Experimental Model of Disease
112
0.300
None
1.000
1
2004
2004
Myotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
19
7
0.100
None
0
Reticulocytosis
phenotype
Pathological Conditions, Signs and Symptoms
Finding
40
1
0.100
None
0
Impaired exercise tolerance
phenotype
Finding
76
7
0.100
None
0
Elevated total bilirubin
phenotype
Finding
17
1
0.100
None
0