| 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 |