C0024623 |
Malignant neoplasm of stomach
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
300 |
14 |
C0038356 |
Stomach Neoplasms
|
group |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Abnormality of the digestive system; Neoplasm
|
297 |
47 |
C1708349 |
Hereditary Diffuse Gastric Cancer
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
293 |
110 |
C0235874 |
Disease Exacerbation
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
|
|
165 |
0 |
C0557874 |
Global developmental delay
|
disease |
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
133 |
505 |
C0424605 |
Developmental delay (disorder)
|
phenotype |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
|
|
37 |
31 |
C0021051 |
Immunologic Deficiency Syndromes
|
group |
Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the immune system
|
23 |
7 |
C3809651 |
INFANTILE LIVER FAILURE SYNDROME 2
|
disease |
|
Disease or Syndrome
|
|
|
1 |
12 |
C1390474 |
Increased susceptibility to fractures
|
phenotype |
|
Finding
|
|
Abnormality of the skeletal system
|
1 |
5 |
C3541319 |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY
|
disease |
|
Disease or Syndrome
|
|
|
1 |
4 |