FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

237872005: Poikilodermal cutaneous amyloid (disorder)


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
356482015 Poikilodermal cutaneous amyloid en Synonym Active Entire term case insensitive SNOMED CT core module
626663011 Poikilodermal cutaneous amyloid (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Poikilodermal cutaneous amyloid Is a Amyloidosis of skin true Inferred relationship Existential restriction modifier
Poikilodermal cutaneous amyloid Is a Localized hereditary amyloidosis true Inferred relationship Existential restriction modifier
Poikilodermal cutaneous amyloid Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Poikilodermal cutaneous amyloid Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier
Poikilodermal cutaneous amyloid Associated morphology Focal amyloid false Inferred relationship Existential restriction modifier 1
Poikilodermal cutaneous amyloid Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Poikilodermal cutaneous amyloid Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier 1
Poikilodermal cutaneous amyloid Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start