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388981000: Congenital dystrophia brevicollis (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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