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722060007: dystrophie musculaire oculo-gastro-intestinale (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330422010 Oculogastrointestinal muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330423017 Oculogastrointestinal muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330424011 Visceral myopathy with familial external ophthalmoplegia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758151000241110 dystrophie musculaire oculo-gastro-intestinale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
901021000172115 syndrome de myopathie viscérale familiale, ophtalmoplégie externe fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
952281000172113 dystrophie musculaire oculo-gastro-intestinale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3330425012 An extremely rare autosomal recessively inherited neuromuscular disease characterized by ocular manifestations such as ptosis and diplopia followed by chronic diarrhea, malnutrition and intestinal pseudo-obstruction. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330426013 An extremely rare autosomal recessively inherited neuromuscular disease characterised by ocular manifestations such as ptosis and diplopia followed by chronic diarrhoea, malnutrition and intestinal pseudo-obstruction. 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
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Congenital anomaly of intestinal tract true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) localisation d'une constatation (attribut) Structure of visual system (body structure) true Inferred relationship Some 1
Oculogastrointestinal muscular dystrophy (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Oculogastrointestinal muscular dystrophy (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Oculogastrointestinal muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculogastrointestinal muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Congenital anomaly of visual system true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Motility disorder of intestine false Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Pseudo-obstruction of intestine true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Digestive system hereditary disorder true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) est un(e) (attribut) Hereditary disorder of the visual system true Inferred relationship Some
Oculogastrointestinal muscular dystrophy (disorder) morphologie associée (attribut) Pseudo-obstruction true Inferred relationship Some 2
Oculogastrointestinal muscular dystrophy (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Oculogastrointestinal muscular dystrophy (disorder) localisation d'une constatation (attribut) intestins true Inferred relationship Some 2
Oculogastrointestinal muscular dystrophy (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Oculogastrointestinal muscular dystrophy (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Oculogastrointestinal muscular dystrophy (disorder) localisation d'une constatation (attribut) Structure of visual system (body structure) false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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