Preferred Name |
Hemoglobin Trait |
|
Synonyms |
Heterozygous Hemoglobinopathy |
|
Definitions |
A condition in which a person is heterozygous for a globin gene, with one normal allele and one defective allele. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C95534 |
|
curator note |
NCIT includes this class below "Hemoglobinopathy", hence its inclusion here. |
|
database cross reference |
NCIT:C95534 |
|
definition |
A condition in which a person is heterozygous for a globin gene, with one normal allele and one defective allele. |
|
definition source | ||
existence in other ontologies |
Sufficient |
|
hasExactSynonym |
Heterozygous Hemoglobinopathy |
|
prefixIRI |
NCIT:C95534 |
|
prefLabel |
Hemoglobin Trait |
|
previous identifier |
SCDO:0000550 |
|
rdfs:label |
Hemoglobin Trait |
|
subClassOf |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/NCIT_C95534 | BERO | SAME_URI | |
http://purl.obolibrary.org/obo/NCIT_C95534 | BERO | LOOM | |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hemoglobin_Trait | CSEO | LOOM | |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C95534 | NCIT | LOOM |