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46659004: Von Hippel-Lindau syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1032261000241115 maladie de von Hippel-Lindau (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
122541000077114 angiomatose rétinocérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
388151000172114 maladie de von Hippel-Lindau fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
4579935012 VHL (Von Hippel-Lindau) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
469301000172110 syndrome de Von Hippel-Lindau fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
494574010 Lindau's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
77765013 Von Hippel-Lindau syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
77766014 Familial cerebello-retinal angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
77767017 Lindau' disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
77768010 Cerebroretinal angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784032018 Von Hippel-Lindau syndrome (disorder) en Fully specified name 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
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) survenue (attribut) congénital true Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Developmental hereditary disorder false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Neoplasm true Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Neoplasm true Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Multisystem disorder (disorder) false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) affection cérébelleuse false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Disorder of brain (disorder) false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Multisystem disorder U-V (navigational concept) false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Disorder of skin AND/OR subcutaneous tissue of head (disorder) false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Neurocutaneous syndrome true Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Congenital anomaly of head false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Congenital hamartosis false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Hamartoma (morphologic abnormality) false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) système nerveux true Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) syndrome familial avec prédisposition aux cancers (trouble) true Inferred relationship Some
maladie de von Hippel-Lindau (trouble) survenue (attribut) congénital true Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) survenue (attribut) congénital false Inferred relationship Some 3
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
maladie de von Hippel-Lindau (trouble) est un(e) (attribut) Hereditary disorder of the integument true Inferred relationship Some
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Neoplasm false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) dysplasie false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 2
maladie de von Hippel-Lindau (trouble) survenue (attribut) congénital false Inferred relationship Some
maladie de von Hippel-Lindau (trouble) localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some 1
maladie de von Hippel-Lindau (trouble) morphologie associée (attribut) Angiomatosis false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of Von Hippel-Lindau syndrome (situation) constatation associée (attribut) True maladie de von Hippel-Lindau (trouble) Inferred relationship Some 1

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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