Preferred Name | Hemoglobinopathy | |
Synonyms |
|
|
Definitions |
An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C3092 |
|
ALT_DEFINITION |
Normal or abnormal findings related to the structural alterations of a globin chain within the hemoglobin molecule. An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule. |
|
code |
C3092 |
|
Contributing_Source |
ACC/AHA CPTAC NICHD |
|
definition |
An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule. |
|
in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 http://purl.obolibrary.org/obo/NCIT_C158520 http://purl.obolibrary.org/obo/NCIT_C156952 http://purl.obolibrary.org/obo/NCIT_C158035 http://purl.obolibrary.org/obo/NCIT_C132009 |
|
label |
Hemoglobinopathy |
|
Legacy Concept Name |
Hemoglobinopathy |
|
Preferred_Name |
Hemoglobinopathy |
|
prefixIRI |
NCIT:C3092 |
|
prefLabel |
Hemoglobinopathy |
|
Semantic_Type |
Disease or Syndrome |
|
UMLS_CUI |
C0019045 |
|
subClassOf |