Sickle Cell Disease Ontology
93 terms(s) returned
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- A Parental Guide to Managing Sickle Cell Disease
- APOL1
- ASCQ-Me - Quality of Care in SCD
- ASCQ-Me Score
- Abdominal Vaso-Occlusive Crisis
- Ability to Carry Out Activities of Daily Living
- Abnormal Biological Process
- Abnormal Hemoglobin
- Abnormal Hemoglobin Level in SCD
- Abnormal Hemoglobin in SCD
- Abnormal Leukocyte Morphology
- Abnormality of Metabolism/Homeostasis
- Abnormality of the Cerebral Vasculature
- Abnormality of the Musculature
- Absence of Alpha Globin Synthesis with Gamma Globin Synthesis
- Absent Hemoglobin A
- Absent Hemoglobin C
- Absent Hemoglobin D-Punjab
- Absent Hemoglobin E
- Absent Hemoglobin G-Philadelphia
- Absent Hemoglobin O-Arab
- Absent Hemoglobin S
- Acetaminophen
- Acide
- Acute Clinical Visit
- Acute Complications of Sickle Cell Disease
- Acute Hepatic Sequestration
- Acute Non-Specific Wheezing Episode
- Acute Phenotype
- Acute Sickle Cell Crisis
- Acute Sickle Cell Pain Management
- Acute Splenic Sequestration Crisis
- Acute Symptomatic Seizure
- Acute Upper Respiratory Tract Infection
- Acutely Severe Anemia
- Adja
- Adjunct Analgesic Agent
- Adrenal Insufficiency
- Adult Hemoglobin
- Adult Migraine Questionnaire
- Adverse Drug Event
- Adverse Event (AE)
- Agarose Gel Electrophoresis
- Aged Neutrophil Count
- Agenesis of Corpus Callosum
- Alanine Aminotransferase Blood Test
- Alanine Aminotransferase Level
- Albuminuria
- Alcohol - Lifetime Use
- Alcohol - Lifetime Use Diagnostic Instrument
