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711407000: Thrombocytopathy, asplenia and miosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3078328015 Stormorken syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3078428016 Thrombocytopathy, asplenia and miosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3078438014 Thrombocytopathy, asplenia and miosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3078583013 Stormorken-Sjaastad-Langslet syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3078328015 Stormorken syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3078428016 Thrombocytopathy, asplenia and miosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3078428016 Thrombocytopathy, asplenia and miosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3078438014 Thrombocytopathy, asplenia and miosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3078438014 Thrombocytopathy, asplenia and miosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3078583013 Stormorken-Sjaastad-Langslet syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
600611000274117 Thrombozytopathie-Asplenie-Miosis-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3409251001000112 Stormorken-Sjaastad-Langslet-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
600611000274117 Thrombozytopathie-Asplenie-Miosis-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3409251001000112 Stormorken-Sjaastad-Langslet-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thrombocytopathy, asplenia and miosis (disorder) Is a Asplenia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopathy, asplenia and miosis (disorder) Is a Congenital miosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopathy, asplenia and miosis (disorder) Is a Thrombocytopenic disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopathy, asplenia and miosis (disorder) Finding site Splenic structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Thrombocytopathy, asplenia and miosis (disorder) Has definitional manifestation Platelet count below reference range (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopathy, asplenia and miosis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopathy, asplenia and miosis (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopathy, asplenia and miosis (disorder) Finding site Iris structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopathy, asplenia and miosis (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Thrombocytopathy, asplenia and miosis (disorder) Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 1
Thrombocytopathy, asplenia and miosis (disorder) Is a Congenital thrombocytopaenia true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopathy, asplenia and miosis (disorder) Finding site Iris structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopathy, asplenia and miosis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopathy, asplenia and miosis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopathy, asplenia and miosis (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopathy, asplenia and miosis (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopathy, asplenia and miosis (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopathy, asplenia and miosis (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 5
Thrombocytopathy, asplenia and miosis (disorder) Finding site Pupil structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Thrombocytopathy, asplenia and miosis (disorder) Interprets Pupil constriction (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopathy, asplenia and miosis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Thrombocytopathy, asplenia and miosis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 5
Thrombocytopathy, asplenia and miosis (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopathy, asplenia and miosis (disorder) Is a Spleen finding true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopathy, asplenia and miosis (disorder) Interprets Size of pupil true Inferred relationship Existential restriction modifier (core metadata concept) 6
Thrombocytopathy, asplenia and miosis (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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