Sickle Cell Disease (SKCA)

Alias:

Sickle Cell Anemia

Hemoglobin Sc Disease

Anemia, Sickle Cell

Hb Ss Disease

Hb-Ss Disease Without Crisis

Sickle Cell Trait

Hereditary Haemoglobinopathy Disorder Homozygous for Haemoglobin S

Hb-S - [sickle Cell Haemoglobin] Carrier

Sickle-Cell/hb-C Disease Without Crisis

Hbas - [sickle Cell Haemoglobin Trait]

Haemoglobin Sickle Cell Trait Disorder

Sickling Disorder Due to Haemoglobin S

Hb-Ss Disease with Vaso-Occlusive Pain

Sickling Disorder Due to Hemoglobin S

Sickle-Cell Trait Haemoglobin Disease

Hemoglobin S Disease Without Crisis

Hbas - [heterozygous Haemoglobin S]

Hb S Disease with Mention of Crisis

Sickle-Cell Anaemia Without Crisis

Haemoglobin Ss Disease with Crisis

Sickle-Cell Heterozygous Disorder

Sickle-Cell Disorder with Crisis

Sickle-Cell Haemoglobin Disease

Sickle-Cell Anaemia with Crisis

Heterozygous Sickle Cell Trait

Sickle Cell Haemoglobin Trait

Sickle-Cell Disease Carrier

Scd - [sickle Cell Disease]

Sca - [sickle Cell Anaemia]

Hb-Ss Disease with Crisis

Haemoglobin a-S Genotype

As - [sickle Cell Trait]

Sickle-Cell Disorder Nos

Sickle Cell Disease Nos

Sickle-Cell Anaemia Nos

Haemoglobin Sc Disease

Haemoglobin Ss Disease

Sickle Cell Disorders

Haemoglobin S Disease

Vaso-Occlusive Crisis

Hemoglobin S Disease

Sickle Cell Disorder

Sickle Cell Syndrome

Sickle Cell Anaemia

Hbss Without Crisis

Sickle Cell Crisis

Hb-S/hb-C Disease

Hbss with Crisis

Herrick Anaemia

Drepanocytosis

Hb Sc Disease

Hb S Disease

Hbs Disease

Skca

Scd

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Sickle Cell Disease, also known as sickle cell anemia, is related to hereditary persistence of fetal hemoglobin-sickle cell disease syndrome and acute chest syndrome, and has symptoms including abdominal pain, angina pectoris and chest pain. An important gene associated with Sickle Cell Disease is HBB (Hemoglobin Subunit Beta), and among its related pathways/superpathways are Glucose / Energy Metabolism and Binding and Uptake of Ligands by Scavenger Receptors. The drugs Sulfadoxine and Pyrimethamine have been mentioned in the context of this disorder. Affiliated tissues include Blood, bone marrow and bone, and related phenotypes are chronic hemolytic anemia and hemolytic anemia

Related ID：

MALACARDS：SCK005

OMIM：603903

MESH：D000755

ICD11：1711513381