Jump to:
loading...| Preferred Name |
Hemoglobin H Disease |
|
| Synonyms |
Hemoglobin H Disease |
|
| Definitions |
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C95504 |
|
| ALT_DEFINITION |
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia. |
|
| code |
C95504 |
|
| Concept_In_Subset | ||
| Contributing_Source |
NICHD |
|
| DEFINITION |
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia. |
|
| FULL_SYN |
Hemoglobin H Disease |
|
| label |
Hemoglobin H Disease |
|
| Preferred_Name |
Hemoglobin H Disease |
|
| prefixIRI |
Thesaurus:C95504 |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C3161174 |
|
| subClassOf |
Create mapping