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716857003: Hereditary pheochromocytoma and paraganglioma (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3307259011 Hereditary pheochromocytoma and paraganglioma (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3307802018 Hereditary pheochromocytoma and paraganglioma en Synonym Active Entire term case insensitive SNOMED CT core module
3308606015 Hereditary phaeochromocytoma and paraganglioma en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary pheochromocytoma and paraganglioma Associated morphology Paraganglioma true Inferred relationship Existential restriction modifier 1
Hereditary pheochromocytoma and paraganglioma Associated morphology Pheochromocytoma true Inferred relationship Existential restriction modifier 2
Hereditary pheochromocytoma and paraganglioma Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary pheochromocytoma and paraganglioma Is a Paraganglioma true Inferred relationship Existential restriction modifier
Hereditary pheochromocytoma and paraganglioma Is a Pheochromocytoma true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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