C0919934 |
Abdominal wall infection
|
disease |
|
Disease or Syndrome
|
|
|
1 |
0 |
C1860224 |
ABLEPHARON-MACROSTOMIA SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
genetic disease; syndrome
|
|
41 |
13 |
C0233514 |
Abnormal behavior
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
820 |
101 |
C0398350 |
Acute cardiac pulmonary edema
|
disease |
|
Disease or Syndrome
|
|
|
6 |
0 |
C0742343 |
Acute Chest Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
405 |
135 |
C0340044 |
Acute exacerbation of chronic obstructive airways disease
|
phenotype |
Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
63 |
1 |
C4040419 |
Acute hypercapnic respiratory failure
|
disease |
|
Disease or Syndrome
|
|
|
3 |
0 |
C0275518 |
Acute infectious disease
|
group |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
|
|
198 |
5 |
C0238990 |
Acute lower respiratory tract infection
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
7 |
0 |
C0238284 |
Acute mountain sickness
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
21 |
3 |
C0155626 |
Acute myocardial infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
765 |
118 |
C4303980 |
Acute on chronic hypercapnic respiratory failure
|
disease |
|
Disease or Syndrome
|
|
|
1 |
0 |
C0264490 |
Acute respiratory failure
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
78 |
5 |
C0339901 |
Acute respiratory infections
|
group |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
35 |
0 |
C0085281 |
Addictive Behavior
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
330 |
54 |
C0001418 |
Adenocarcinoma
|
group |
Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
2080 |
167 |
C0220597 |
Adult Hodgkin Lymphoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
396 |
27 |
C0699949 |
airway disease
|
disease |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
198 |
1 |
C0001883 |
Airway Obstruction
|
group |
Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
104 |
5 |
C0233826 |
Akatamathesia
|
disease |
|
Mental or Behavioral Dysfunction
|
|
|
1 |
0 |
C0155877 |
Allergic asthma
|
disease |
Respiratory Tract Diseases; Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
371 |
55 |
C2607914 |
Allergic rhinitis (disorder)
|
disease |
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the immune system; Abnormality of head or neck
|
394 |
96 |
C3662483 |
Allergic sensitization
|
disease |
|
Disease or Syndrome
|
|
|
79 |
16 |
C0221757 |
alpha 1-Antitrypsin Deficiency
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
73 |
6 |
C0002871 |
Anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of blood and blood-forming tissues
|
573 |
79 |