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388981000: Congenital dystrophia brevicollis (disorder)


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
1463159012 Congenital dystrophia brevicollis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character case insensitive (core metadata concept) SNOMED CT core
1493576014 Nielsen's disease 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 Only initial character case insensitive (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 Switzerland NRC maintained Module
369831000077112 brevicollis congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dystrophia brevicollis (disorder) Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Is a Congenital anomaly of cervical vertebra true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophia brevicollis (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophia brevicollis (disorder) Finding site Bone structure of cervical vertebra true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophia brevicollis (disorder) Is a Lesion of neck true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Is a Congenital fusion of spine true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophia brevicollis (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophia brevicollis (disorder) Associated morphology Abnormally fused structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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