Hyperinsulinemic hypoglycemia, familial, 3
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
11
|
0.700 |
strong |
1.000 |
9 |
11
|
1998 |
2017 |
Fasting hyperglycaemia
|
phenotype |
|
Finding
|
1
|
|
0.300 |
strong |
|
0 |
|
|
|
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
|
disease |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Iatrogenic hyperinsulinism
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hyperinsulinemic hypoglycemia, familial, 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
3
|
147
|
0.300 |
None |
1.000 |
1 |
|
2004 |
2004 |
Hyperinsulinemic hypoglycemia, familial, 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
3
|
50
|
0.300 |
None |
1.000 |
1 |
|
2004 |
2004 |
Abnormality of the autonomic nervous system
|
phenotype |
|
Anatomical Abnormality
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Loss of hypoglycemic warning
|
disease |
|
Disease or Syndrome
|
4
|
1
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Diabetes in youth
|
disease |
|
Disease or Syndrome
|
4
|
2
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Disorder of carbohydrate metabolism
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Transient hypothyroxinaemia of prematurity
|
disease |
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Beta-cell dysfunction
|
phenotype |
|
Finding
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Mitochondrial Diabetes
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Reduced pancreatic beta cells
|
phenotype |
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Diabetes mellitus autosomal dominant type II (disorder)
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
8
|
139
|
1.000 |
strong |
1.000 |
82 |
137
|
1992 |
2019 |
maternal hyperglycemia
|
disease |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Disease or Syndrome
|
8
|
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2018 |
K ATP Permanent Neonatal Diabetes
|
disease |
|
Disease or Syndrome
|
8
|
2
|
0.020 |
None |
1.000 |
2 |
1
|
2014 |
2015 |
Hypoglycaemic episode
|
disease |
|
Disease or Syndrome
|
8
|
2
|
0.010 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
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
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Fasting hyperinsulinemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
10
|
|
0.100 |
None |
|
0 |
|
|
|
Limb joint contracture
|
phenotype |
|
Finding
|
10
|
1
|
0.100 |
None |
|
0 |
|
|
|
Neonatal insulin-dependent diabetes mellitus
|
phenotype |
|
Finding
|
10
|
6
|
0.100 |
None |
|
0 |
|
|
|
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
12
|
48
|
0.060 |
None |
1.000 |
6 |
|
1997 |
2014 |
Caudal Regression Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
12
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Nesidioblastosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
12
|
|
0.200 |
None |
|
0 |
|
|
|