Jump to:
loading...| Preferred Name |
Anemia_due_to_Membrane_Defect |
|
| Synonyms |
|
|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Anemia_due_to_Membrane_Defect |
|
| ID |
C101218 |
|
| NCI_Definition |
A group of inherited hemolytic anemias caused by erythrocyte membrane defects. This includes hereditary pyropoikilocytosis, hereditary spherocytosis and hereditary elliptocytosis. |
|
| NCI_PT |
Hemolytic Anemia due to Membrane Defect |
|
| NICHD_Definition |
_ |
|
| prefixIRI |
Anemia_due_to_Membrane_Defect |
|
| prefLabel |
Anemia_due_to_Membrane_Defect |
|
| Subset_Association1 |
NICHD Pediatric Terminology |
|
| Subset_Association2 |
Neonatal Research Network Terminology |
|
| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Hemolytic_Anemia |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SNOMEDCT/111575000 | SNOMEDCT | LOOM |