loading...| Preferred Name |
Sickle Cell-Hemoglobin D Disease |
|
| Synonyms |
Hemoglobin SD Disease Sickle Cell-Hemoglobin D Disease |
|
| Definitions |
A variant of sickle cell disease due to heterozygosity for hemoglobin S and hemoglobin D mutations. Patients present with the symptoms of sickle cell disease but the symptoms are less frequent and severe compared to patients with hemoglobin SS disease. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C155310 |
|
| code |
C155310 |
|
| DEFINITION |
A variant of sickle cell disease due to heterozygosity for hemoglobin S and hemoglobin D mutations. Patients present with the symptoms of sickle cell disease but the symptoms are less frequent and severe compared to patients with hemoglobin SS disease. |
|
| FULL_SYN |
Hemoglobin SD Disease Sickle Cell-Hemoglobin D Disease |
|
| label |
Sickle Cell-Hemoglobin D Disease |
|
| Preferred_Name |
Sickle Cell-Hemoglobin D Disease |
|
| prefixIRI |
Thesaurus:C155310 |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C0272084 |
|
| subClassOf |