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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Extracutaneous mastocytoma | |
| Synonyms |
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| Definitions |
A rare neoplastic disease characterized by a localized, unifocal, low-grade tumor composed of mature mast cells, without evidence of systemic mastocytosis or skin lesions. The tumor most commonly arises in the lung and shows a non-destructive growth pattern. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_66662 |
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| definition |
A rare neoplastic disease characterized by a localized, unifocal, low-grade tumor composed of mature mast cells, without evidence of systemic mastocytosis or skin lesions. The tumor most commonly arises in the lung and shows a non-destructive growth pattern.
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| definition_citation |
Orphanet
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=66662 |
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| hasDbXref |
ICD-10:C96.2 ICD-11:2A21.3 UMLS:C0272202
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| label |
Extracutaneous mastocytoma
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| notation |
ORPHA:66662
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_66662
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| prefLabel |
Extracutaneous mastocytoma
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| treeView | ||
| subClassOf |
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