FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

388981000: brevicollis congénital (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1463159012 Congenital dystrophia brevicollis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1483042010 Congenital dystrophia brevicollis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1493576014 Nielsen's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1493577017 Bonnevie-Ullrich and Klippel-Feil syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
369831000077112 brevicollis congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
656951000077119 brevicollis congénital (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dystrophia brevicollis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Autosomal hereditary disorder true Inferred relationship Some
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Congenital disease false Inferred relationship Some
Congenital dystrophia brevicollis (disorder) survenue (attribut) congénital false Inferred relationship Some
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Congenital anomaly of cervical vertebra true Inferred relationship Some
Congenital dystrophia brevicollis (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital dystrophia brevicollis (disorder) morphologie associée (attribut) Congenital abnormal fusion true Inferred relationship Some 1
Congenital dystrophia brevicollis (disorder) localisation d'une constatation (attribut) vertèbre cervicale (structure corporelle) true Inferred relationship Some 1
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Lesion of neck true Inferred relationship Some
Congenital dystrophia brevicollis (disorder) est un(e) (attribut) Congenital fusion of spine true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start