C0373595 |
Creatinine clearance measurement
|
phenotype |
|
Laboratory Procedure
|
|
|
0 |
51 |
C0030305 |
Pancreatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the digestive system; Abnormality of the immune system
|
0 |
6 |
C0030809 |
Pemphigus Vulgaris
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
0 |
6 |
C0523708 |
5-Hydroxyindoleacetic acid measurement
|
phenotype |
|
Laboratory Procedure
|
|
|
0 |
5 |
C0021364 |
Male infertility
|
phenotype |
Male Urogenital Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the genitourinary system
|
0 |
4 |
C0751908 |
Vestibular Neuronitis
|
disease |
Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
0 |
4 |
C1720994 |
Eye Movement Measurements
|
phenotype |
|
Diagnostic Procedure
|
|
|
0 |
4 |
C0024419 |
Waldenstrom Macroglobulinemia
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Neoplastic Process
|
genetic disease; disease of metabolism; disease of anatomical entity; disease of cellular proliferation
|
Abnormality of metabolism/homeostasis; Abnormality of the immune system; Neoplasm; Abnormal cellular phenotype; Abnormality of blood and blood-forming tissues
|
0 |
3 |
C0085215 |
Ovarian Failure, Premature
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
0 |
3 |
C0020450 |
Hyperemesis Gravidarum
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
|
Sign or Symptom
|
|
Abnormality of prenatal development or birth
|
0 |
2 |
C0025874 |
Metrorrhagia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
|
Abnormality of the genitourinary system; Abnormality of the endocrine system
|
0 |
2 |
C0030807 |
Pemphigus
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
0 |
2 |
C0227791 |
Vaginal Discharge
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Finding
|
disease of anatomical entity
|
|
0 |
2 |
C0263313 |
Pemphigus Foliaceus
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
|
|
0 |
2 |
C0373785 |
Thrombomodulin Assay
|
phenotype |
|
Laboratory Procedure
|
|
|
0 |
2 |
C0456103 |
Sepsis of the newborn
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections
|
Disease or Syndrome
|
|
Abnormality of the immune system
|
0 |
2 |
C0523807 |
Oxygen saturation measurement
|
phenotype |
|
Laboratory Procedure
|
|
|
0 |
2 |
C0557163 |
Household income
|
phenotype |
|
Finding
|
|
|
0 |
2 |
C1168401 |
Squamous cell carcinoma of the head and neck
|
disease |
Neoplasms
|
Neoplastic Process
|
disease of cellular proliferation
|
|
0 |
2 |
C1332201 |
Adult Diffuse Large B-Cell Lymphoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
0 |
2 |
C1838604 |
EPILEPSY, CHILDHOOD ABSENCE, 1
|
disease |
|
Disease or Syndrome
|
|
|
0 |
2 |
C2609414 |
Acute kidney injury
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Injury or Poisoning
|
disease of anatomical entity
|
Abnormality of the genitourinary system
|
0 |
2 |
C3827961 |
Spontaneous Preterm Birth
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Finding
|
|
|
0 |
2 |
C0003615 |
Appendicitis
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
disease of anatomical entity
|
|
0 |
1 |
C0010073 |
Coronary Artery Vasospasm
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
0 |
1 |