C0000731 |
Abdomen distended
|
phenotype |
Digestive System Diseases
|
Finding
|
|
Abnormality of the digestive system
|
0 |
6 |
C0000737 |
Abdominal Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
|
Abnormality of the digestive system; Constitutional symptom
|
1 |
11 |
C0000744 |
Abetalipoproteinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
Abnormality of metabolism/homeostasis
|
1 |
16 |
C0000768 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
|
|
11 |
0 |
C0000771 |
Abnormalities, Drug-Induced
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
|
|
5 |
0 |
C0000772 |
Multiple congenital anomalies
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
|
|
17 |
350 |
C0000786 |
Spontaneous abortion
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
|
Abnormality of prenatal development or birth
|
109 |
0 |
C0000809 |
Abortion, Habitual
|
disease |
Female Urogenital Diseases and Pregnancy Complications
|
Disease or Syndrome
|
|
|
2 |
0 |
C0000821 |
Threatened abortion
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
disease of anatomical entity
|
|
1 |
0 |
C0000822 |
Abortion, Tubal
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
|
|
109 |
0 |
C0000832 |
Abruptio Placentae
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
disease of anatomical entity
|
Abnormality of prenatal development or birth
|
3 |
0 |
C0000889 |
Acanthosis Nigricans
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the integument
|
0 |
4 |
C0001080 |
Achondroplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
genetic disease; disease of anatomical entity
|
|
1 |
9 |
C0001122 |
Acidosis
|
phenotype |
Nutritional and Metabolic Diseases
|
Pathologic Function
|
disease of metabolism
|
Abnormality of metabolism/homeostasis
|
2 |
0 |
C0001125 |
Acidosis, Lactic
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
disease of metabolism
|
Abnormality of metabolism/homeostasis
|
6 |
14 |
C0001126 |
Renal tubular acidosis
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
|
4 |
1 |
C0001144 |
Acne Vulgaris
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
4 |
30 |
C0001175 |
Acquired Immunodeficiency Syndrome
|
group |
Infections; Immune System Diseases
|
Disease or Syndrome
|
disease by infectious agent
|
|
3 |
28 |
C0001193 |
Apert syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
genetic disease; disease of anatomical entity; syndrome
|
|
2 |
14 |
C0001197 |
Acrodermatitis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
3 |
0 |
C0001206 |
Acromegaly
|
disease |
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the nervous system; Abnormality of the endocrine system
|
5 |
0 |
C0001231 |
ACTH Syndrome, Ectopic
|
disease |
Neoplasms
|
Disease or Syndrome
|
disease of anatomical entity
|
|
1 |
0 |
C0001338 |
Herpetic Acute Necrotizing Encephalitis
|
disease |
Infections; Nervous System Diseases
|
Disease or Syndrome
|
|
|
5 |
0 |
C0001349 |
Acute-Phase Reaction
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
|
|
1 |
0 |
C0001364 |
Massive Hepatic Necrosis
|
phenotype |
Digestive System Diseases
|
Pathologic Function
|
|
|
2 |
0 |