Preferred Name |
Sickle_Cell-Beta-Thalassemia |
|
Synonyms |
|
|
ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Sickle_Cell-Beta-Thalassemia |
|
ID |
C95539 |
|
NCI_Definition |
A heterozygous state in which a person has a hemoglobin S allele along with a beta-thalassemia allele. The severity of the condition is determined to a large extent by the quantity of normal hemoglobin produced by the beta-thalassemia gene. |
|
NCI_PT |
Sickle Beta Thalassemia |
|
NICHD_Definition |
_ |
|
prefixIRI |
Sickle_Cell-Beta-Thalassemia |
|
prefLabel |
Sickle_Cell-Beta-Thalassemia |
|
Subset_Association1 |
NICHD Pediatric Terminology |
|
Subset_Association2 |
Neonatal Research Network Terminology |
|
SYN | ||
subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Thalassemia |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/SNOMEDCT/127041004 | SNOMEDCT | LOOM | |
http://purl.bioontology.org/ontology/MEDDRA/10055579 | MEDDRA | LOOM |