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771187008: Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3704819016 Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3704820010 Arthropathy camptodactyly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3704821014 Pericarditis, arthropathy, camptodactyly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3704822019 Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3704823012 Jacobs syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3704824018 CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3704825017 CACP 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
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Is a Flexion deformity of finger false Inferred relationship Existential restriction modifier
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Finding site Proximal interphalangeal joint of finger structure true Inferred relationship Existential restriction modifier 1
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Is a Polyarthropathy true Inferred relationship Existential restriction modifier
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Associated morphology Flexion deformity false Inferred relationship Existential restriction modifier 1
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Finding site Joint structure of multiple body sites true Inferred relationship Existential restriction modifier 2
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Associated morphology Fixed flexion deformity true Inferred relationship Existential restriction modifier 1
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome Is a Fixed flexion deformity finger 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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