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189814006: Pancreatoblastoma (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2722977018 Pancreatoblastoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
291682019 Pancreatoblastoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4574184017 A rare neoplastic gastroenterologic disease most often found in children, which usually presents with the non-specific symptoms of a palpable mass, vomiting, abdominal pain, jaundice, and weight loss/failure to thrive. Histologically, this malignant epithelial pancreatic neoplasm of the exocrine cells has multiple lines of differentiation (acinar, ductal, mesenchymal, neuroendocrine) and the presence of squamoid nests. Pancreatoblastoma can occur in any part of the pancreas. It is a malignant embryonal neoplasm that seems to recapitulate the embryogenesis of the pancreas, presumably because it originates from the pluripotent pancreatic stem cells during foregut development. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pancreatoblastoma (disorder) localisation d'une constatation (attribut) structure du pancréas true Inferred relationship Some 1
Pancreatoblastoma (disorder) est un(e) (attribut) Primary malignant neoplasm of pancreas (disorder) true Inferred relationship Some
Pancreatoblastoma (disorder) morphologie associée (attribut) Pancreatoblastoma (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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