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loading...| Preferred Name |
Sickle Cell-Hemoglobin D Disease |
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| Synonyms |
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| 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. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C155310 |
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| code |
C155310 |
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| 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. |
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| label |
Sickle Cell-Hemoglobin D Disease |
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| Preferred_Name |
Sickle Cell-Hemoglobin D Disease |
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| prefixIRI |
NCIT:C155310 |
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| prefLabel |
Sickle Cell-Hemoglobin D Disease |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0272084 |
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| subClassOf |
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