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771471002: syndrome d'oedème du nerf optique-splénomégalie (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3706353012 Optic nerve edema, splenomegaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706354018 Optic nerve oedema, splenomegaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706355017 Optic nerve edema, splenomegaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
770771000241118 syndrome d'oedème du nerf optique-splénomégalie (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
942641000172116 syndrome d'oedème du nerf optique-splénomégalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3706356016 A rare presumably genetic disorder characterized by idiopathic massive splenomegaly with pancytopenia and childhood-onset chronic optic nerve edema with slowly progressive vision loss. Additional reported features include anhidrosis, urticaria and headaches. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706357013 A rare presumably genetic disorder characterised by idiopathic massive splenomegaly with pancytopenia and childhood-onset chronic optic nerve oedema with slowly progressive vision loss. Additional reported features include anhidrosis, urticaria and headaches. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Optic nerve edema, splenomegaly syndrome (disorder) est un(e) (attribut) Hereditary disorder of the visual system false Inferred relationship Some
Optic nerve edema, splenomegaly syndrome (disorder) est un(e) (attribut) splénomégalie true Inferred relationship Some
Optic nerve edema, splenomegaly syndrome (disorder) localisation d'une constatation (attribut) Optic nerve structure true Inferred relationship Some 1
Optic nerve edema, splenomegaly syndrome (disorder) morphologie associée (attribut) Edema true Inferred relationship Some 1
Optic nerve edema, splenomegaly syndrome (disorder) morphologie associée (attribut) Enlargement (morphologic abnormality) true Inferred relationship Some 2
Optic nerve edema, splenomegaly syndrome (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Optic nerve edema, splenomegaly syndrome (disorder) est un(e) (attribut) Inherited optic neuropathy true Inferred relationship Some
Optic nerve edema, splenomegaly syndrome (disorder) survenue (attribut) enfance true Inferred relationship Some 1
Optic nerve edema, splenomegaly syndrome (disorder) localisation d'une constatation (attribut) Entire spleen true Inferred relationship Some 2
Optic nerve edema, splenomegaly syndrome (disorder) est un(e) (attribut) Disorder characterized by edema true Inferred relationship Some
Optic nerve edema, splenomegaly syndrome (disorder) est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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