Preferred Name |
Hemoglobinopathy |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3092 |
ALT_DEFINITION |
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. |
code |
C3092 |
Concept_In_Subset | |
Contributing_Source |
NICHD |
DEFINITION |
An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule. |
FULL_SYN |
Hemoglobinopathies / Iron Metabolism |
Has_NICHD_Parent | |
label |
Hemoglobinopathy |
Legacy_Concept_Name |
Hemoglobinopathy |
NICHD_Hierarchy_Term |
Hemoglobinopathy |
Preferred_Name |
Hemoglobinopathy |
prefixIRI |
C3092 |
prefLabel |
Hemoglobinopathy |
Semantic_Type |
Disease or Syndrome |
UMLS_CUI |
C0019045 |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/DOID_2860 | Human Disease Ontology 123 | LOOM |