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loading...| Preferred Name |
Histiocytic_Syndrome |
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| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Histiocytic_Syndrome |
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| ID |
C3107 |
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| NCI_Definition |
A neoplastic proliferation of Langerhans cells which contain Birbeck granules by ultrastructural examination. Three major overlapping syndromes are recognized: eosinophilic granuloma, Letterer-Siwe disease, and Hand-Schuller-Christian disease. The clinical course is generally related to the number of organs affected at presentation. (WHO, 2001) |
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| NCI_PT |
Langerhans Cell Histiocytosis |
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| NICHD_Definition |
_ |
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| prefixIRI |
Histiocytic_Syndrome |
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| prefLabel |
Histiocytic_Syndrome |
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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#Neoplasm |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SNOMEDCT/127068004 | SNOMEDCT | LOOM | |
| http://purl.bioontology.org/ontology/RCD/X20E5 | RCD | LOOM |