C1306459 |
Primary malignant neoplasm
|
group |
Neoplasms
|
Neoplastic Process
|
disease of cellular proliferation
|
|
8221 |
1374 |
C0596263 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
|
|
6243 |
355 |
C0009402 |
Colorectal Carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
5473 |
1962 |
C0024623 |
Malignant neoplasm of stomach
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
3806 |
615 |
C0235974 |
Pancreatic carcinoma
|
disease |
Digestive System Diseases; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
2689 |
322 |
C0011847 |
Diabetes
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
disease of metabolism
|
|
2359 |
710 |
C0030567 |
Parkinson Disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
2078 |
990 |
C2931822 |
Nasopharyngeal carcinoma
|
disease |
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
1553 |
320 |
C0000768 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
|
|
1098 |
73 |
C0400966 |
Non-alcoholic Fatty Liver Disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
1058 |
222 |
C2919142 |
Short Stature, CTCAE
|
phenotype |
|
Finding
|
|
|
1010 |
0 |
C0008925 |
Cleft Palate
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
|
Congenital Abnormality
|
syndrome; physical disorder
|
|
611 |
158 |
C0033377 |
Ptosis
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
|
|
607 |
12 |
C0271650 |
Impaired glucose tolerance
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
disease of metabolism
|
|
596 |
81 |
C0149678 |
Epstein-Barr Virus Infections
|
group |
Infections
|
Disease or Syndrome
|
|
|
384 |
72 |
C0016842 |
Congenital pectus excavatum
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
|
|
272 |
36 |
C1306503 |
Congenital exomphalos
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
disease of anatomical entity; physical disorder
|
|
235 |
0 |
C0376634 |
Craniofacial Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
|
|
234 |
4 |
C1845977 |
X- linked recessive
|
phenotype |
|
Finding
|
|
|
172 |
1 |
C0544886 |
Somatic mutation
|
phenotype |
|
Cell or Molecular Dysfunction
|
|
|
151 |
0 |
C1858430 |
Death in infancy
|
phenotype |
|
Finding
|
|
|
146 |
7 |
C0576226 |
Short foot
|
phenotype |
|
Finding
|
|
|
116 |
0 |
C2347762 |
Childhood Teratoma
|
disease |
Neoplasms
|
Neoplastic Process
|
|
|
95 |
3 |
C1368898 |
Adult Teratoma
|
disease |
Neoplasms
|
Neoplastic Process
|
disease of cellular proliferation
|
|
93 |
3 |
C0005941 |
Bone Diseases, Developmental
|
group |
Musculoskeletal Diseases
|
Disease or Syndrome
|
|
|
82 |
2 |