Scleroderma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
316
|
5
|
0.100 |
None |
|
0 |
|
|
|
Fragile skin
|
phenotype |
|
Finding
|
26
|
5
|
0.100 |
None |
|
0 |
|
|
|
Liver carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
5725
|
942
|
0.100 |
None |
|
0 |
|
|
|
Facial Hypertrichosis
|
phenotype |
Skin and Connective Tissue Diseases
|
Finding
|
8
|
2
|
0.100 |
None |
|
0 |
|
|
|
Thin skin
|
phenotype |
|
Finding
|
77
|
4
|
0.100 |
None |
|
0 |
|
|
|
Onycholysis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Anemia, Hemolytic
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
154
|
31
|
0.100 |
None |
|
0 |
|
|
|
Photosensitivity of skin
|
phenotype |
Skin and Connective Tissue Diseases
|
Pathologic Function
|
91
|
3
|
0.100 |
None |
|
0 |
|
|
|
Hyperpigmentation in sun-exposed areas
|
phenotype |
Skin and Connective Tissue Diseases
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Alopecia
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
491
|
375
|
0.100 |
None |
|
0 |
|
|
|
Systemic Scleroderma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
979
|
287
|
0.100 |
None |
|
0 |
|
|
|
Cirrhosis
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
919
|
110
|
0.100 |
None |
|
0 |
|
|
|
Hemochromatosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
93
|
45
|
0.010 |
None |
< 0.001 |
1 |
|
1998 |
1998 |
Systemic Inflammatory Response Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
185
|
9
|
0.010 |
None |
< 0.001 |
1 |
|
2017 |
2017 |
HEMOCHROMATOSIS, TYPE 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
83
|
62
|
0.010 |
None |
< 0.001 |
1 |
|
1998 |
1998 |
Congenital diaphragmatic hernia
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
239
|
31
|
0.010 |
None |
< 0.001 |
1 |
|
2000 |
2000 |
Glaucoma, Primary Open Angle
|
disease |
Eye Diseases
|
Disease or Syndrome
|
383
|
222
|
0.010 |
None |
< 0.001 |
1 |
|
2018 |
2018 |
Imprinting error
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
< 0.001 |
1 |
|
2006 |
2006 |
Paternal uniparental disomy of chromosome 20
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
< 0.001 |
1 |
|
2018 |
2018 |
Uroporphyrinogen decarboxylase deficiency
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
|
0.020 |
None |
0.500 |
2 |
|
1998 |
2019 |
Bacteremia
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
233
|
7
|
0.020 |
None |
0.500 |
2 |
|
2017 |
2017 |
Malignant Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
8621
|
1641
|
0.020 |
None |
0.500 |
2 |
|
2011 |
2019 |
Primary malignant neoplasm
|
group |
Neoplasms
|
Neoplastic Process
|
8221
|
1374
|
0.020 |
None |
0.500 |
2 |
|
2011 |
2019 |
Beckwith-Wiedemann Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
107
|
84
|
0.040 |
None |
0.750 |
4 |
|
1999 |
2011 |
Sporadic porphyria cutanea tarda
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
4
|
3
|
0.050 |
None |
0.800 |
5 |
|
1985 |
2002 |