×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0
Pruritus
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Finding
107
2
0.100
None
0
Hypertriglyceridemia
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
340
169
0.100
None
0
Erythema
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
227
8
0.100
None
0
Iron-Refractory Iron Deficiency Anemia
disease
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
51
36
0.100
None
0
Decreased liver function
phenotype
Finding
59
5
0.100
None
0
Eczema
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
863
368
0.100
None
0
Cholelithiasis
disease
Digestive System Diseases
Disease or Syndrome
252
90
0.100
None
0
Anemia, Hemolytic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
154
31
0.100
None
0
Childhood onset
phenotype
Finding
56
0.100
None
0
Photosensitivity of skin
phenotype
Skin and Connective Tissue Diseases
Pathologic Function
91
3
0.100
None
0
Lymphangitis carcinomatosa
disease
Neoplasms
Neoplastic Process
7
0.010
None
< 0.001
1
2019
2019
Erythropoietic Protoporphyria
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
24
3
0.800
strong
0.992
125
3
1977
2020
PROTOPORPHYRIA, ERYTHROPOIETIC, 1
disease
Disease or Syndrome
1
25
0.600
None
1.000
21
25
1991
2017
Liver diseases
group
Digestive System Diseases
Disease or Syndrome
1019
100
0.080
None
1.000
8
1994
2009
Ferrochelatase deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
4
0.300
None
1.000
6
1999
2018
Disorders of Porphyrin Metabolism
group
Nutritional and Metabolic Diseases
Disease or Syndrome
26
7
0.040
None
1.000
4
1982
2016
Neoplasms
group
Neoplasms
Neoplastic Process
10161
1644
0.040
None
1.000
4
2004
2019
Liver Failure
disease
Digestive System Diseases
Disease or Syndrome
293
20
0.140
None
1.000
4
1993
2009
Porphyria, Erythropoietic
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
20
26
0.030
None
1.000
3
1999
2019
Variegate Porphyria
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
21
24
0.030
None
1.000
3
1977
2002
MYELODYSPLASTIC SYNDROME
group
Hemic and Lymphatic Diseases
Neoplastic Process
1033
95
0.030
None
1.000
3
2006
2017
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
0.030
None
1.000
3
1999
2019
Malignant neoplasm of breast
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6941
3417
0.030
None
1.000
3
1999
2019
Malignant tumor of colon
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
2969
688
0.020
None
1.000
2
2008
2017