Preferred Name |
Alpha Thalassemia |
|
Synonyms |
|
|
Definitions |
A genetic hematologic disorder characterized by partial or complete absence of the alpha globin chains of the heme molecule. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C34368 |
|
ALT_DEFINITION |
A genetic hematologic disorder characterized by loss of function mutations in one or more of the alpha globin genes. |
|
code |
C34368 |
|
Contributing_Source |
Cellosaurus NICHD |
|
definition |
A genetic hematologic disorder characterized by partial or complete absence of the alpha globin chains of the heme molecule. |
|
in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 |
|
label |
Alpha Thalassemia |
|
Legacy Concept Name |
Alpha_Thalassemia |
|
Preferred_Name |
Alpha Thalassemia |
|
prefixIRI |
NCIT:C34368 |
|
prefLabel |
Alpha Thalassemia |
|
Semantic_Type |
Disease or Syndrome |
|
UMLS_CUI |
C0002312 |
|
subClassOf |
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