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190905008: Cystic fibrosis (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
293528019 Cystic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
293529010 CF - Cystic fibrosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
293530017 Fibrocystic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
293531018 CF en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
293532013 Mucoviscidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
374961000172111 mucoviscidose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
524021000241110 mucoviscidose (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
559221000172113 fibrose kystique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
574544017 Cystic fibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

12 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cystic fibrosis est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Cystic fibrosis est un(e) (attribut) Disorder of respiratory system (disorder) false Inferred relationship Some
Cystic fibrosis est un(e) (attribut) Inherited mucociliary clearance defect true Inferred relationship Some
Cystic fibrosis localisation d'une constatation (attribut) structure de l'appareil respiratoire false Inferred relationship Some
Cystic fibrosis a pour interprétation (attribut) altéré true Inferred relationship Some 1
Cystic fibrosis interprète (attribut) Mucociliary clearance true Inferred relationship Some 1
Cystic fibrosis morphologie associée (attribut) Defect true Inferred relationship Some 2
Cystic fibrosis localisation d'une constatation (attribut) structure des voies respiratoires true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Distal intestinal obstruction syndrome due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 2
Perinatal jaundice due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 1
Cystic fibrosis without meconium ileus est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Cystic fibrosis with meconium ileus est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Cystic fibrosis of the lung est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Diabetes mellitus due to cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 2
Liver disease due to cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 1
Diabetes mellitus co-occurrent and due to cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 3
mucoviscidose non soupçonnée constatation associée (attribut) False Cystic fibrosis Inferred relationship Some 1
Suspected cystic fibrosis (situation) constatation associée (attribut) False Cystic fibrosis Inferred relationship Some 1
Cystic fibrosis with no meconium ileus est un(e) (attribut) False Cystic fibrosis Inferred relationship Some
Cystic fibrosis with pulmonary manifestations est un(e) (attribut) False Cystic fibrosis Inferred relationship Some
Cystic fibrosis with intestinal manifestations est un(e) (attribut) False Cystic fibrosis Inferred relationship Some
Family history of cystic fibrosis (situation) constatation associée (attribut) True Cystic fibrosis Inferred relationship Some 1
Suspected cystic fibrosis (situation) constatation associée (attribut) True Cystic fibrosis Inferred relationship Some 1
mucoviscidose non soupçonnée constatation associée (attribut) True Cystic fibrosis Inferred relationship Some 1
Cystic fibrosis screening a pour objet (attribut) False Cystic fibrosis Inferred relationship Some 1
Cystic fibrosis screening test a pour objet (attribut) False Cystic fibrosis Inferred relationship Some
Family history of cystic fibrosis (situation) constatation associée (attribut) False Cystic fibrosis Inferred relationship Some 1
Fibrosing colonopathy (disorder) associé à (attribut) False Cystic fibrosis Inferred relationship Some 2
Nasal potential difference test (procedure) a pour objet (attribut) True Cystic fibrosis Inferred relationship Some 2
Cystic fibrosis NOS est un(e) (attribut) False Cystic fibrosis Inferred relationship Some
Cystic fibrosis with other manifestations est un(e) (attribut) False Cystic fibrosis Inferred relationship Some
Diabetes mellitus co-occurrent and due to cystic fibrosis (disorder) associé à (attribut) False Cystic fibrosis Inferred relationship Some
Arthropathy associated with cystic fibrosis associé à (attribut) True Cystic fibrosis Inferred relationship Some 1
Elevated liver enzymes level due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 1
Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 3
Portal hypertension due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 1
Osteoporosis due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 1
Male infertility due to cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 1
Otorhinolaryngological manifestation co-occurrent and due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 1
Digestive system manifestation co-occurrent and due to cystic fibrosis Due to True Cystic fibrosis Inferred relationship Some 1
Female infertility due to cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 1
Follicular hamartoma with alopecia and cystic fibrosis syndrome (disorder) est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Cystic fibrosis of pancreas est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder) est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Polyneuropathy due to classical cystic fibrosis (disorder) Due to True Cystic fibrosis Inferred relationship Some 2
Fetal cystic fibrosis (disorder) est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Diabetes mellitus co-occurrent and due to cystic fibrosis (disorder) est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Classical cystic fibrosis (disorder) est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Atypical cystic fibrosis (disorder) est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Subclinical cystic fibrosis est un(e) (attribut) True Cystic fibrosis Inferred relationship Some
Family history of cystic fibrosis (situation) constatation associée (attribut) False Cystic fibrosis Inferred relationship Some 1
Cystic fibrosis screening a pour objet (attribut) True Cystic fibrosis Inferred relationship Some 2

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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