Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
10344015 | Klippel-Feil sequence | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
10345019 | Klippel-Feil syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
10346018 | Klippel-Feil deformity | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
10347010 | Cervical vertebral fusion syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
10348017 | Cervical vertebral fusion | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
794476018 | Klippel-Feil sequence (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
1231552013 | Cervical fusion syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
1231553015 | KFS - Klippel-Feil syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Wilderwanck's syndrome | Is a | False | Klippel-Feil sequence | Inferred relationship | Existential restriction modifier | |
Klippel-Feil syndrome NOS | Is a | False | Klippel-Feil sequence | Inferred relationship | Existential restriction modifier | |
Wildervanck syndrome | Is a | True | Klippel-Feil sequence | Inferred relationship | Existential restriction modifier | |
Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome | Is a | True | Klippel-Feil sequence | Inferred relationship | Existential restriction modifier | |
Klippel-Feil syndrome NOS | Is a | False | Klippel-Feil sequence | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets