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loading...| Preferred Name | Primary_Immune_Deficiency_Disorder | |
| Synonyms |
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|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Primary_Immune_Deficiency_Disorder |
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| ID |
C3131 |
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| NCI_Definition |
Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. |
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| NCI_PT |
Immunodeficiency Syndrome |
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| NICHD_Definition |
Primary immunodeficiencies are disorders in which part of the body's immune system is missing or does not function properly. Most primary immunodeficiencies are genetic disorders; the majority are diagnosed in children under the age of one, although milder forms may not be recognized until adulthood. |
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| prefixIRI |
Primary_Immune_Deficiency_Disorder |
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| prefLabel |
Primary_Immune_Deficiency_Disorder |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Immunolymphatic_System_Disorder |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SNOMEDCT/58606001 | SNOMEDCT | LOOM |