Dilated superficial abdominal veins
|
phenotype |
|
Anatomical Abnormality
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal large intestine physiology
|
phenotype |
|
Anatomical Abnormality
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Elevated alkaline phosphatase of hepatic origin
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Spider hemangioma
|
disease |
|
Disease or Syndrome
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Palmar telangiectasia
|
disease |
|
Anatomical Abnormality
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Polyclonal elevation of IgM
|
phenotype |
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Osteodystrophy
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome; Congenital Abnormality
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
VATER/VACTERL ASSOCIATION
|
disease |
|
Disease or Syndrome
|
8
|
2
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Corneal dystrophy, Fuchs' endothelial, 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
9
|
7
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Chromosome 2q37 deletion syndrome
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Albright's hereditary osteodystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
22
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Nociceptive Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
25
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Chronic Liver Failure
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
25
|
1
|
0.100 |
None |
|
0 |
|
|
|
Pseudohypoparathyroidism, Type Ia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
30
|
20
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Prothrombin time increased
|
phenotype |
Hemic and Lymphatic Diseases
|
Finding
|
30
|
|
0.100 |
None |
|
0 |
|
|
|
social stress
|
disease |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
45
|
22
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
gallbladder neoplasm
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
51
|
6
|
0.100 |
None |
|
0 |
|
|
|
Generalized amyotrophy
|
disease |
|
Disease or Syndrome
|
56
|
6
|
0.100 |
None |
|
0 |
|
|
|
Autoimmune state
|
phenotype |
|
Pathologic Function
|
70
|
|
0.100 |
None |
|
0 |
|
|
|
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
|
disease |
|
Finding
|
82
|
141
|
0.100 |
None |
1.000 |
1 |
1
|
2015 |
2015 |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
|
disease |
|
Disease or Syndrome
|
82
|
142
|
0.100 |
None |
1.000 |
1 |
1
|
2015 |
2015 |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
|
disease |
|
Disease or Syndrome
|
82
|
132
|
0.100 |
None |
1.000 |
1 |
1
|
2015 |
2015 |
Fuchs Endothelial Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
94
|
32
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Thyroiditis
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
104
|
7
|
0.100 |
None |
|
0 |
|
|
|
Pruritus
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Finding
|
107
|
2
|
0.100 |
None |
|
0 |
|
|
|