C4721773 |
Postoperative cognitive dysfunction
|
phenotype |
|
Mental or Behavioral Dysfunction
|
|
|
3 |
C4553639 |
Arterial Injury, CTCAE
|
phenotype |
|
Finding
|
|
|
4 |
C4552089 |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
3 |
C4551527 |
Focal segmental glomerulosclerosis 1
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
1 |
C4551463 |
Colon adenoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
|
|
1 |
C4540036 |
FRASER SYNDROME 2
|
disease |
|
Disease or Syndrome
|
genetic disease
|
|
1 |
C4277682 |
Chemical and Drug Induced Liver Injury
|
disease |
Digestive System Diseases; Chemically-Induced Disorders
|
Disease or Syndrome
|
|
|
44 |
C4054127 |
Radiation Nephropathy
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
|
|
2 |
C4048195 |
Autosomal dominant hypocalcemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
3 |
C3887915 |
AERODIGESTIVE TRACT CANCER, SQUAMOUS CELL, ALCOHOL-RELATED, PROTECTION AGAINST
|
phenotype |
|
Finding
|
disease of mental health
|
|
2 |
C3887892 |
Aortic Valve Disease 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
1 |
C3850141 |
Acute-On-Chronic Liver Failure
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
|
|
2 |
C3825727 |
Respiratory allergy
|
phenotype |
|
Pathologic Function
|
|
|
1 |
C3809278 |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
|
disease |
|
Disease or Syndrome
|
disease of anatomical entity
|
|
1 |
C3805040 |
Phospholipidosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
|
|
1 |
C3715128 |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
3 |
C3714630 |
Respirovirus Infections
|
disease |
Infections
|
Disease or Syndrome
|
|
|
1 |
C3714509 |
Nutrition Disorders
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
disease of metabolism
|
|
1 |
C3711385 |
Deoxyguanosine Kinase Deficiency
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
1 |
C3665444 |
Neutrophilia (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
|
|
1 |
C3665419 |
intracranial glioma
|
disease |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
|
|
7 |
C3658208 |
Dysbiosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
|
|
1 |
C3495676 |
Anorectal Malformations
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
Abnormality of the digestive system
|
6 |
C3489856 |
Cold Hypersensitivity
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
|
|
1 |
C3278923 |
Dilated ventricles (finding)
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
1 |