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232336001: Paget's disease of skin (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
348089016 Paget's disease of skin en Synonym Active Entire term case sensitive SNOMED CT core module
620388015 Paget's disease of skin (morphologic abnormality) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2842040017 Paget disease of skin en Synonym Active Entire term case sensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Paget's disease of skin Is a Ductal, lobular AND/OR medullary neoplasm true Inferred relationship Existential restriction modifier
Paget's disease of skin Is a Malignant neoplasm, primary false Inferred relationship Existential restriction modifier
Paget's disease of skin Is a Malignant neoplasm with apocrine differentiation true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Extramammary Paget's disease Is a False Paget's disease of skin Inferred relationship Existential restriction modifier
Paget's disease, mammary Is a True Paget's disease of skin Inferred relationship Existential restriction modifier
Paget's disease, extramammary (except Paget's disease of bone) Is a True Paget's disease of skin Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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