Central neuroblastoma
|
disease |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
2419
|
231
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Deformity
|
group |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Anatomical Abnormality
|
350
|
26
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Aplasia Cutis Congenita
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
393
|
14
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Childhood Burkitt Lymphoma
|
disease |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
477
|
7
|
0.010 |
None |
1.000 |
1 |
|
1985 |
1985 |
Adult Burkitt Lymphoma
|
disease |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
475
|
7
|
0.010 |
None |
1.000 |
1 |
|
1985 |
1985 |
Inflammatory Breast Carcinoma
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
183
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Non-small cell lung cancer stage I
|
disease |
|
Neoplastic Process
|
115
|
1
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Chronic viral hepatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
59
|
8
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Familial lichen amyloidosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
230
|
24
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Fibrosis of pancreas
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
72
|
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Acute hepatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
62
|
2
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Congenital hypoplasia of lung
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Congenital Abnormality
|
175
|
6
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Rieger syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
23
|
7
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Thickening of pleura
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
25
|
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Disseminated eosinophilic collagen disease
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
14
|
2
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Chronic ulcer
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
15
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Tumor necrosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Neoplastic Process
|
350
|
1
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Carcinoid tumor no ICD-O subtype
|
phenotype |
Neoplasms
|
Neoplastic Process
|
122
|
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Malignant neoplasm of gastrointestinal tract
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
423
|
55
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Progressive Neoplastic Disease
|
phenotype |
|
Neoplastic Process
|
384
|
40
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Epithelial ovarian cancer
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Neoplastic Process
|
1224
|
129
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Malignant neoplasm of esophagus
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
1286
|
214
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Chronic small plaque psoriasis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
82
|
3
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Dysplastic oral leukoplakia
|
disease |
Pathological Conditions, Signs and Symptoms; Neoplasms; Stomatognathic Diseases
|
Neoplastic Process
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Developmental absence of tooth
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
41
|
15
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |