Cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
878
|
124
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Anastomosis
|
disease |
|
Acquired Abnormality
|
155
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Skin callus
|
disease |
Skin and Connective Tissue Diseases
|
Acquired Abnormality
|
154
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Polycystic Kidney - body part
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Anatomical Abnormality
|
54
|
1
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Abnormality of the metaphysis
|
disease |
|
Anatomical Abnormality
|
97
|
|
0.100 |
None |
|
0 |
|
|
|
Single umbilical artery
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
28
|
5
|
0.100 |
None |
1.000 |
4 |
1
|
1976 |
2004 |
Dysmorphic features
|
disease |
|
Congenital Abnormality
|
439
|
617
|
0.100 |
None |
1.000 |
3 |
2
|
2010 |
2017 |
Patent ductus arteriosus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
510
|
56
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Congenital diaphragmatic hernia
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
239
|
31
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Deficiency of steroid 21-monooxygenase
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
54
|
26
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Familial idiopathic hypercalciuria
|
disease |
Pathological Conditions, Signs and Symptoms
|
Congenital Abnormality
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Liver hyperplasia
|
disease |
|
Congenital Abnormality
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Osteoglophonic dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
100
|
4
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
50
|
62
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
PATENT DUCTUS ARTERIOSUS 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
229
|
12
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
1261
|
77
|
0.100 |
None |
|
0 |
|
|
|
Hypocalciuric hypercalcemia, familial, type 1
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
46
|
58
|
1.000 |
None |
0.993 |
145 |
44
|
1976 |
2020 |
Familial benign hypercalcemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
24
|
35
|
0.700 |
None |
0.989 |
88 |
34
|
1991 |
2018 |
Hypercalcemia
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
157
|
9
|
0.500 |
None |
0.955 |
67 |
6
|
1976 |
2020 |
Hypoparathyroidism - autosomal dominant
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
12
|
44
|
0.190 |
None |
0.981 |
53 |
43
|
1991 |
2016 |
HYPERPARATHYROIDISM, NEONATAL SEVERE
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
|
Disease or Syndrome
|
14
|
14
|
0.800 |
strong |
0.962 |
52 |
14
|
1995 |
2020 |
Autosomal dominant hypocalcemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
29
|
9
|
0.700 |
None |
1.000 |
51 |
5
|
1995 |
2019 |
Hyperparathyroidism, Primary
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
115
|
39
|
0.200 |
None |
0.941 |
34 |
5
|
2001 |
2019 |
Cytokine Release Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Chemically-Induced Disorders
|
Disease or Syndrome
|
29
|
|
0.100 |
None |
1.000 |
32 |
|
2016 |
2020 |
Hyperparathyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
111
|
14
|
0.700 |
None |
0.966 |
29 |
6
|
1996 |
2019 |