C2930930 |
Abdominal obesity metabolic syndrome
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
|
|
1 |
C0000737 |
Abdominal Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
|
Abnormality of the digestive system; Constitutional symptom
|
1 |
C0000880 |
Acanthamoeba Keratitis
|
disease |
Infections; Eye Diseases
|
Disease or Syndrome
|
|
|
1 |
C0001249 |
Actinobacillus Infections
|
disease |
Infections
|
Disease or Syndrome
|
disease of anatomical entity; disease by infectious agent
|
|
1 |
C0149514 |
Acute bronchitis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the respiratory system
|
1 |
C0023479 |
Acute myelomonocytic leukemia
|
disease |
Neoplasms
|
Neoplastic Process
|
|
Abnormality of the immune system; Neoplasm; Abnormality of blood and blood-forming tissues
|
1 |
C0023487 |
Acute Promyelocytic Leukemia
|
disease |
Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Abnormality of the immune system; Neoplasm; Abnormality of blood and blood-forming tissues
|
1 |
C1735373 |
Acute uveitis
|
disease |
|
Disease or Syndrome
|
|
|
1 |
C0032580 |
Adenomatous Polyposis Coli
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
genetic disease
|
|
1 |
C0041755 |
Adverse reaction to drug
|
group |
Chemically-Induced Disorders
|
Pathologic Function
|
|
|
1 |
C0041228 |
African Trypanosomiasis
|
disease |
Infections
|
Disease or Syndrome
|
disease by infectious agent
|
|
1 |
C0001849 |
AIDS Dementia Complex
|
disease |
Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
|
|
1 |
C0078911 |
AIDS-Associated Nephropathy
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases; Immune System Diseases
|
Disease or Syndrome
|
|
|
1 |
C2717792 |
Airway Remodeling
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
|
|
1 |
C0001916 |
Albinism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
Abnormality of the integument
|
1 |
C0078918 |
Albinism, Oculocutaneous
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
genetic disease
|
|
1 |
C0270985 |
Alcohol myopathy
|
disease |
Musculoskeletal Diseases; Nervous System Diseases; Chemically-Induced Disorders; Mental Disorders
|
Disease or Syndrome
|
|
|
1 |
C0751865 |
Alcohol-Induced Disorders, Nervous System
|
disease |
Nervous System Diseases; Chemically-Induced Disorders
|
Disease or Syndrome
|
|
|
1 |
C0559469 |
Allergy to eggs
|
phenotype |
Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
1 |
C0205710 |
Alpers Syndrome (disorder)
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism; disease of anatomical entity
|
|
1 |
C0002351 |
Altitude Sickness
|
phenotype |
Respiratory Tract Diseases
|
Disease or Syndrome
|
|
|
1 |
C0002418 |
Amblyopia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the eye
|
1 |
C0039585 |
Androgen-Insensitivity Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
1 |
C0002895 |
Anemia, Sickle Cell
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
1 |
C0178417 |
Anhedonia
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
1 |