FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

238783008: Familial pigmented purpuric eruption (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
357881010 Familial pigmented purpuric eruption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
357882015 Familial capillaritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
627710019 Familial pigmented purpuric eruption (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
357881010 Familial pigmented purpuric eruption en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
357881010 Familial pigmented purpuric eruption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
357882015 Familial capillaritis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
357882015 Familial capillaritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
627710019 Familial pigmented purpuric eruption (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
627710019 Familial pigmented purpuric eruption (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5025631000241119 éruption purpurique pigmentée familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5025631000241119 éruption purpurique pigmentée familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial pigmented purpuric eruption (disorder) Is a Capillaritis false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Associated morphology Purpura false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Finding site Structure of capillary blood vessel false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial pigmented purpuric eruption (disorder) Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Finding site Peripheral vascular system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Finding site Blood vessel structure of skin (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Is a Disorder of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial pigmented purpuric eruption (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial pigmented purpuric eruption (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial pigmented purpuric eruption (disorder) Finding site Structure of capillary blood vessel false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial pigmented purpuric eruption (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial pigmented purpuric eruption (disorder) Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Is a Papular eruption false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Associated morphology Papular rash true Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial pigmented purpuric eruption (disorder) Is a Skin deposits (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Is a Disorder of skin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Is a Purpuric disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial pigmented purpuric eruption (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial pigmented purpuric eruption (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Familial pigmented purpuric eruption (disorder) Associated morphology Purpura true Inferred relationship Existential restriction modifier (core metadata concept) 4
Familial pigmented purpuric eruption (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 5
Familial pigmented purpuric eruption (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 5
Familial pigmented purpuric eruption (disorder) Associated morphology Hemosiderin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial pigmented purpuric eruption (disorder) Finding site Structure of capillary of skin true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial pigmented purpuric eruption (disorder) Is a Pigmented purpuric dermatosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial pigmented purpuric eruption (disorder) Clinical course Chronic (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start